Ce • cet publication inclut la propriété intellectuelle couverte par les déclarations suivantes.
It is a condition of HGNC funding from NIH and the Welcome Trust that the nomenclature and information provided is freely available to all. Anyone may use the HGNC data, but we request that they reference the "HUGO Gene Nomenclature Committee at the European Bioinformatics Institute"
and the website where possible.
This material contains content that is copyright of SNOMED International. Implementers of these specifications must have the appropriate SNOMED CT Affiliate license - for more information contact https://www.snomed.org/get-snomed
or info@snomed.org
.
Structural unit composed of a nucleic acid molecule which controls its own replication through the interaction of specific proteins at one or more origins of replication ( SO:0000340
).
The definition of variant here originates from Sequence ontology ( variant_of
). This element can represent amino acid or nucleic sequence change(including insertion,deletion,SNP,etc.) It can represent some complex mutation or segment variation with the assist of CIGAR string.
An allele is one of a set of coexisting sequence variants of a gene ( SO:0001023
). Nucleotide(s)/amino acids from start position of sequence to stop position of sequence on the positive (+) strand of the observed sequence. When the sequence type is DNA, it should be the sequence on the positive (+) strand. This will lay in the range between variant.start and variant.end.
An allele is one of a set of coexisting sequence variants of a gene ( SO:0001023
). Nucleotide(s)/amino acids from start position of sequence to stop position of sequence on the positive (+) strand of the reference sequence. When the sequence type is DNA, it should be the sequence on the positive (+) strand. This will lay in the range between variant.start and variant.end.
Unless not suitable, these codes SHALL be taken from For example codes, see
WHO ATC - IPS http://hl7.org/fhir/ValueSet/medication-codes
( extensible
to http://hl7.org/fhir/uv/ips/ValueSet/whoatc-uv-ips
)
What medication was taken Slice: Unordered, Open by type:$this Binding:
WHO ATC - IPS (extensible) ele-1: All FHIR elements must have a @value or children
The FHIR osiris implementation guide has been generated using FSH and the FHIR publisher. Source files including FSH files are available open source on
github
. You can also download the
FHIR NPM Package
.
The OSIRIS project is mainly financed by the
INCA
(Institut National du Cancer, The French National Cancer Institute). The core contributors to the original data model are Institut Curie, Institut Bergonié, the oncology center Léon Bérard, with the contribution of a dozen oncology centre and French hospitals. The current FHIR version of the data model was realized by the same stakeholders in partnership with the start-up
Arkhn
.
The OSIRIS project is mainly financed by the
INCA
(Institut National du Cancer, The French National Cancer Institute). The core contributors to the original data model are Institut Curie, Institut Bergonié, the oncology center Léon Bérard, with the contribution of a dozen oncology centre and French hospitals. The current FHIR version of the data model was realized by the same stakeholders in partnership with the start-up
Arkhn
.
(
extensible
)
