@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP369708.RA5p83cfq7hGShDlr475dycuqr2VGLXdiGI6FxR2-1L0w
> .
@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/eco.owl#
> .
@prefix wi: <
http://purl.org/ontology/wi/core#
> .
@prefix prov: <
http://www.w3.org/ns/prov#
> .
@prefix pav: <
http://purl.org/pav/2.0/
> .
@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/nanopublications.trig#
> .
@prefix dgn-gda: <
http://rdf.disgenet.org/gene-disease-association.ttl#
> .
@prefix dgn-void: <
http://rdf.disgenet.org/v2.1.0/void.ttl#
> .
dgn-np:NP369708.RA5p83cfq7hGShDlr475dycuqr2VGLXdiGI6FxR2-1L0w130_head
{
this:
np:hasAssertion
dgn-np:NP369708.RA5p83cfq7hGShDlr475dycuqr2VGLXdiGI6FxR2-1L0w130_assertion
;
np:hasProvenance
dgn-np:NP369708.RA5p83cfq7hGShDlr475dycuqr2VGLXdiGI6FxR2-1L0w130_provenance
;
np:hasPublicationInfo
dgn-np:NP369708.RA5p83cfq7hGShDlr475dycuqr2VGLXdiGI6FxR2-1L0w130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP369708.RA5p83cfq7hGShDlr475dycuqr2VGLXdiGI6FxR2-1L0w130_assertion
a
np:Assertion
.
dgn-np:NP369708.RA5p83cfq7hGShDlr475dycuqr2VGLXdiGI6FxR2-1L0w130_provenance
a
np:Provenance
.
dgn-np:NP369708.RA5p83cfq7hGShDlr475dycuqr2VGLXdiGI6FxR2-1L0w130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP369708.RA5p83cfq7hGShDlr475dycuqr2VGLXdiGI6FxR2-1L0w130_assertion
{
miriam-gene:673
a
ncit:C16612
.
lld:C0686619
a
ncit:C7057
.
dgn-gda:DGNd1445723dba59968ef8d8121e08723de
sio:SIO_000628
miriam-gene:673
,
lld:C0686619
;
a
sio:SIO_001121
.
}
dgn-np:NP369708.RA5p83cfq7hGShDlr475dycuqr2VGLXdiGI6FxR2-1L0w130_provenance
{
dgn-np:NP369708.RA5p83cfq7hGShDlr475dycuqr2VGLXdiGI6FxR2-1L0w130_assertion
dcterms:description
"[Subtype stratification demonstrated that the BRAF V600E mutation was associated with tumor size, extrathyroid invasion, the presence of lymph node metastasis and risk of disease recurrence, and mortality in patients with the classic variant of PTC.]. 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:19152441
;
prov:wasDerivedFrom
dgn-void:befree-20140225
;
prov:wasGeneratedBy
eco:ECO_0000203
.
dgn-void:befree-20140225
pav:importedOn
"2014-02-25"^^
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:NP369708.RA5p83cfq7hGShDlr475dycuqr2VGLXdiGI6FxR2-1L0w130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:35:36+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:disgenetrdf
;
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
"v2.1.0.0" .
dgn-void:disgenetrdf
pav:version
"v2.1.0" .
}