@prefix this: <
http://rdf.disgenet.org/resource/nanopub/NP466746.RA_XCNcph6z-pwSpEIZgXqctor5v3luyIaFH8uqQ3LT2E
> .
@prefix rdfs: <
http://www.w3.org/2000/01/rdf-schema#
> .
@prefix xsd: <
http://www.w3.org/2001/XMLSchema#
> .
@prefix sio: <
http://semanticscience.org/resource/
> .
@prefix ncit: <
http://ncicb.nci.nih.gov/xml/owl/EVS/Thesaurus.owl#
> .
@prefix lld: <
http://linkedlifedata.com/resource/umls/id/
> .
@prefix miriam-gene: <
http://identifiers.org/ncbigene/
> .
@prefix miriam-pubmed: <
http://identifiers.org/pubmed/
> .
@prefix eco: <
http://purl.obolibrary.org/obo/
> .
@prefix wi: <
http://purl.org/ontology/wi/core#
> .
@prefix prov: <
http://www.w3.org/ns/prov#
> .
@prefix pav: <
http://purl.org/pav/
> .
@prefix prv: <
http://purl.org/net/provenance/ns#
> .
@prefix dcterms: <
http://purl.org/dc/terms/
> .
@prefix np: <
http://www.nanopub.org/nschema#
> .
@prefix dgn-np: <
http://rdf.disgenet.org/resource/nanopub/
> .
@prefix dgn-gda: <
http://rdf.disgenet.org/resource/gda/
> .
@prefix dgn-void: <
http://rdf.disgenet.org/v4.0.0/void/
> .
dgn-np:NP466746.RA_XCNcph6z-pwSpEIZgXqctor5v3luyIaFH8uqQ3LT2E130_head
{
this:
np:hasAssertion
dgn-np:NP466746.RA_XCNcph6z-pwSpEIZgXqctor5v3luyIaFH8uqQ3LT2E130_assertion
;
np:hasProvenance
dgn-np:NP466746.RA_XCNcph6z-pwSpEIZgXqctor5v3luyIaFH8uqQ3LT2E130_provenance
;
np:hasPublicationInfo
dgn-np:NP466746.RA_XCNcph6z-pwSpEIZgXqctor5v3luyIaFH8uqQ3LT2E130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP466746.RA_XCNcph6z-pwSpEIZgXqctor5v3luyIaFH8uqQ3LT2E130_assertion
a
np:Assertion
.
dgn-np:NP466746.RA_XCNcph6z-pwSpEIZgXqctor5v3luyIaFH8uqQ3LT2E130_provenance
a
np:Provenance
.
dgn-np:NP466746.RA_XCNcph6z-pwSpEIZgXqctor5v3luyIaFH8uqQ3LT2E130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP466746.RA_XCNcph6z-pwSpEIZgXqctor5v3luyIaFH8uqQ3LT2E130_assertion
{
miriam-gene:5979
a
ncit:C16612
.
lld:C0238462
a
ncit:C7057
.
dgn-gda:DGN7d541e4f6ac5335349d778b17151bc65
sio:SIO_000628
miriam-gene:5979
,
lld:C0238462
;
a
sio:SIO_001121
.
}
dgn-np:NP466746.RA_XCNcph6z-pwSpEIZgXqctor5v3luyIaFH8uqQ3LT2E130_provenance
{
dgn-np:NP466746.RA_XCNcph6z-pwSpEIZgXqctor5v3luyIaFH8uqQ3LT2E130_assertion
dcterms:description
"[In hereditary medullary thyroid carcinoma (MTC), recommendations regarding timing and extent of surgery are mainly based on the data of patients with the codon 634 RET mutation, which is the most often affected codon.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine."@en ;
wi:evidence
dgn-void:source_evidence_literature
;
sio:SIO_000772
miriam-pubmed:15517481
;
prov:wasDerivedFrom
dgn-void:befree-2016
;
prov:wasGeneratedBy
eco:ECO_0000203
.
dgn-void:befree-2016
pav:importedOn
"2016-02-19"^^
xsd:date
.
dgn-void:source_evidence_literature
a
eco:ECO_0000212
;
rdfs:comment
"Gene-disease associations inferred from text-mining the literature."@en ;
rdfs:label
"DisGeNET evidence - LITERATURE"@en .
}
dgn-np:NP466746.RA_XCNcph6z-pwSpEIZgXqctor5v3luyIaFH8uqQ3LT2E130_publicationInfo
{
this:
dcterms:created
"2016-05-13T12:45:16+02:00"^^
xsd:dateTime
;
dcterms:rights
<
http://opendatacommons.org/licenses/odbl/1.0/
> ;
dcterms:rightsHolder
dgn-void:IBIGroup
;
dcterms:subject
sio:SIO_000983
;
prv:usedData
dgn-void:disgenetv3.0rdf
;
pav:authoredBy
<
http://orcid.org/0000-0001-5999-6269
> , <
http://orcid.org/0000-0002-7534-7661
> , <
http://orcid.org/0000-0002-9383-528X
> , <
http://orcid.org/0000-0003-0169-8159
> , <
http://orcid.org/0000-0003-1244-7654
> ;
pav:createdBy
<
http://orcid.org/0000-0003-0169-8159
> ;
pav:version
"v4.0.0.0" .
dgn-void:disgenetv3.0rdf
pav:version
"v4.0.0" .
}