@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP361828.RAKhx0sCQZ-aWvx_vO6pMuEmxBwikMIJMuQwZIP8m-3Gg
> .
@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:NP361828.RAKhx0sCQZ-aWvx_vO6pMuEmxBwikMIJMuQwZIP8m-3Gg130_head
{
this:
np:hasAssertion
dgn-np:NP361828.RAKhx0sCQZ-aWvx_vO6pMuEmxBwikMIJMuQwZIP8m-3Gg130_assertion
;
np:hasProvenance
dgn-np:NP361828.RAKhx0sCQZ-aWvx_vO6pMuEmxBwikMIJMuQwZIP8m-3Gg130_provenance
;
np:hasPublicationInfo
dgn-np:NP361828.RAKhx0sCQZ-aWvx_vO6pMuEmxBwikMIJMuQwZIP8m-3Gg130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP361828.RAKhx0sCQZ-aWvx_vO6pMuEmxBwikMIJMuQwZIP8m-3Gg130_assertion
a
np:Assertion
.
dgn-np:NP361828.RAKhx0sCQZ-aWvx_vO6pMuEmxBwikMIJMuQwZIP8m-3Gg130_provenance
a
np:Provenance
.
dgn-np:NP361828.RAKhx0sCQZ-aWvx_vO6pMuEmxBwikMIJMuQwZIP8m-3Gg130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP361828.RAKhx0sCQZ-aWvx_vO6pMuEmxBwikMIJMuQwZIP8m-3Gg130_assertion
{
miriam-gene:3845
a
ncit:C16612
.
lld:C0029925
a
ncit:C7057
.
dgn-gda:DGN1411e7c7a83fcf91aef5ad6b54165e0b
sio:SIO_000628
miriam-gene:3845
,
lld:C0029925
;
a
sio:SIO_001121
.
}
dgn-np:NP361828.RAKhx0sCQZ-aWvx_vO6pMuEmxBwikMIJMuQwZIP8m-3Gg130_provenance
{
dgn-np:NP361828.RAKhx0sCQZ-aWvx_vO6pMuEmxBwikMIJMuQwZIP8m-3Gg130_assertion
dcterms:description
"[The goals of this study were to perform a comprehensive assessment of the prevalence of KRAS oncogene mutations in invasive epithelial ovarian carcinomas of various histologic subtypes, and for any subgroup(s) in which KRAS mutation was found to be common, to address the hypothesis that those tumors without KRAS mutation had sustained alternative activation of this signaling pathway through mutation of the BRAF oncogene.]. 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:12893203
;
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:NP361828.RAKhx0sCQZ-aWvx_vO6pMuEmxBwikMIJMuQwZIP8m-3Gg130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:35:32+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" .
}