@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP693300.RATr5XxbXRXGvhz_rkkuKqeYToRaLH-R91i36B4QANals
> .
@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:NP693300.RATr5XxbXRXGvhz_rkkuKqeYToRaLH-R91i36B4QANals130_head
{
this:
np:hasAssertion
dgn-np:NP693300.RATr5XxbXRXGvhz_rkkuKqeYToRaLH-R91i36B4QANals130_assertion
;
np:hasProvenance
dgn-np:NP693300.RATr5XxbXRXGvhz_rkkuKqeYToRaLH-R91i36B4QANals130_provenance
;
np:hasPublicationInfo
dgn-np:NP693300.RATr5XxbXRXGvhz_rkkuKqeYToRaLH-R91i36B4QANals130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP693300.RATr5XxbXRXGvhz_rkkuKqeYToRaLH-R91i36B4QANals130_assertion
a
np:Assertion
.
dgn-np:NP693300.RATr5XxbXRXGvhz_rkkuKqeYToRaLH-R91i36B4QANals130_provenance
a
np:Provenance
.
dgn-np:NP693300.RATr5XxbXRXGvhz_rkkuKqeYToRaLH-R91i36B4QANals130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP693300.RATr5XxbXRXGvhz_rkkuKqeYToRaLH-R91i36B4QANals130_assertion
{
miriam-gene:5290
a
ncit:C16612
.
lld:C0919267
a
ncit:C7057
.
dgn-gda:DGN0a64f2008d728b9257fd0abdfe2e3129
sio:SIO_000628
miriam-gene:5290
,
lld:C0919267
;
a
sio:SIO_001121
.
}
dgn-np:NP693300.RATr5XxbXRXGvhz_rkkuKqeYToRaLH-R91i36B4QANals130_provenance
{
dgn-np:NP693300.RATr5XxbXRXGvhz_rkkuKqeYToRaLH-R91i36B4QANals130_assertion
dcterms:description
"[Our data showed mutual exclusivity between the molecular event of PIK3CA amplification and mutations in PIK3CA, KRAS, BRAF genes, which suggests that each of these alterations may individually be sufficient to drive ovarian tumor pathogenesis independently.]. 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:19638206
;
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:NP693300.RATr5XxbXRXGvhz_rkkuKqeYToRaLH-R91i36B4QANals130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:39:01+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" .
}