@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP187636.RAPwUEpsK8cg7AuMUOjMNmzArwrBXcvgcIqufuaseIzss
> .
@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:NP187636.RAPwUEpsK8cg7AuMUOjMNmzArwrBXcvgcIqufuaseIzss130_head
{
this:
np:hasAssertion
dgn-np:NP187636.RAPwUEpsK8cg7AuMUOjMNmzArwrBXcvgcIqufuaseIzss130_assertion
;
np:hasProvenance
dgn-np:NP187636.RAPwUEpsK8cg7AuMUOjMNmzArwrBXcvgcIqufuaseIzss130_provenance
;
np:hasPublicationInfo
dgn-np:NP187636.RAPwUEpsK8cg7AuMUOjMNmzArwrBXcvgcIqufuaseIzss130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP187636.RAPwUEpsK8cg7AuMUOjMNmzArwrBXcvgcIqufuaseIzss130_assertion
a
np:Assertion
.
dgn-np:NP187636.RAPwUEpsK8cg7AuMUOjMNmzArwrBXcvgcIqufuaseIzss130_provenance
a
np:Provenance
.
dgn-np:NP187636.RAPwUEpsK8cg7AuMUOjMNmzArwrBXcvgcIqufuaseIzss130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP187636.RAPwUEpsK8cg7AuMUOjMNmzArwrBXcvgcIqufuaseIzss130_assertion
{
miriam-gene:1956
a
ncit:C16612
.
lld:C0235974
a
ncit:C7057
.
dgn-gda:DGN87e7192c46bfae99232af100edf69130
sio:SIO_000628
miriam-gene:1956
,
lld:C0235974
;
a
sio:SIO_001121
.
}
dgn-np:NP187636.RAPwUEpsK8cg7AuMUOjMNmzArwrBXcvgcIqufuaseIzss130_provenance
{
dgn-np:NP187636.RAPwUEpsK8cg7AuMUOjMNmzArwrBXcvgcIqufuaseIzss130_assertion
dcterms:description
"[The prevalence of the transcriptionally functional EGFR, Src, and Stat3 nuclear complex provides an additional and novel mechanism for supporting the pancreatic cancer phenotype and explains in part the insensitivity of pancreatic cancer cells to the inhibition of EGFR, Src or Stat3 alone.]. 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:21573184
;
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:NP187636.RAPwUEpsK8cg7AuMUOjMNmzArwrBXcvgcIqufuaseIzss130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:33:43+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" .
}