@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP260388.RAh6GOL1m69aI-gfCCuLKIArOVEk8rt_RkHqxlc_XkhsI
> .
@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:NP260388.RAh6GOL1m69aI-gfCCuLKIArOVEk8rt_RkHqxlc_XkhsI130_head
{
this:
np:hasAssertion
dgn-np:NP260388.RAh6GOL1m69aI-gfCCuLKIArOVEk8rt_RkHqxlc_XkhsI130_assertion
;
np:hasProvenance
dgn-np:NP260388.RAh6GOL1m69aI-gfCCuLKIArOVEk8rt_RkHqxlc_XkhsI130_provenance
;
np:hasPublicationInfo
dgn-np:NP260388.RAh6GOL1m69aI-gfCCuLKIArOVEk8rt_RkHqxlc_XkhsI130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP260388.RAh6GOL1m69aI-gfCCuLKIArOVEk8rt_RkHqxlc_XkhsI130_assertion
a
np:Assertion
.
dgn-np:NP260388.RAh6GOL1m69aI-gfCCuLKIArOVEk8rt_RkHqxlc_XkhsI130_provenance
a
np:Provenance
.
dgn-np:NP260388.RAh6GOL1m69aI-gfCCuLKIArOVEk8rt_RkHqxlc_XkhsI130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP260388.RAh6GOL1m69aI-gfCCuLKIArOVEk8rt_RkHqxlc_XkhsI130_assertion
{
miriam-gene:7430
a
ncit:C16612
.
lld:C0238198
a
ncit:C7057
.
dgn-gda:DGNde629e2f84f6161934b26feaee967e91
sio:SIO_000628
miriam-gene:7430
,
lld:C0238198
;
a
sio:SIO_001121
.
}
dgn-np:NP260388.RAh6GOL1m69aI-gfCCuLKIArOVEk8rt_RkHqxlc_XkhsI130_provenance
{
dgn-np:NP260388.RAh6GOL1m69aI-gfCCuLKIArOVEk8rt_RkHqxlc_XkhsI130_assertion
dcterms:description
"[Differentially expressed genes included ezrin, p70S6K, and PKCs, which are known to have key roles in KIT or PDGFRA signaling, and which might therefore contribute to the distinctive clinicopathological features in GISTs with different mutation types.]. 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:15326474
;
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:NP260388.RAh6GOL1m69aI-gfCCuLKIArOVEk8rt_RkHqxlc_XkhsI130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:34:25+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" .
}