@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP231252.RAob6UGXmgIfmj9WPlFt0alQR1eYRVXJvgoV7RAgnSQy4
> .
@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:NP231252.RAob6UGXmgIfmj9WPlFt0alQR1eYRVXJvgoV7RAgnSQy4130_head
{
this:
np:hasAssertion
dgn-np:NP231252.RAob6UGXmgIfmj9WPlFt0alQR1eYRVXJvgoV7RAgnSQy4130_assertion
;
np:hasProvenance
dgn-np:NP231252.RAob6UGXmgIfmj9WPlFt0alQR1eYRVXJvgoV7RAgnSQy4130_provenance
;
np:hasPublicationInfo
dgn-np:NP231252.RAob6UGXmgIfmj9WPlFt0alQR1eYRVXJvgoV7RAgnSQy4130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP231252.RAob6UGXmgIfmj9WPlFt0alQR1eYRVXJvgoV7RAgnSQy4130_assertion
a
np:Assertion
.
dgn-np:NP231252.RAob6UGXmgIfmj9WPlFt0alQR1eYRVXJvgoV7RAgnSQy4130_provenance
a
np:Provenance
.
dgn-np:NP231252.RAob6UGXmgIfmj9WPlFt0alQR1eYRVXJvgoV7RAgnSQy4130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP231252.RAob6UGXmgIfmj9WPlFt0alQR1eYRVXJvgoV7RAgnSQy4130_assertion
{
miriam-gene:3815
a
ncit:C16612
.
lld:C0027627
a
ncit:C7057
.
dgn-gda:DGN0a8a01ce44ec16f072a145afb8f90b76
sio:SIO_000628
miriam-gene:3815
,
lld:C0027627
;
a
sio:SIO_001121
.
}
dgn-np:NP231252.RAob6UGXmgIfmj9WPlFt0alQR1eYRVXJvgoV7RAgnSQy4130_provenance
{
dgn-np:NP231252.RAob6UGXmgIfmj9WPlFt0alQR1eYRVXJvgoV7RAgnSQy4130_assertion
dcterms:description
"[Gene mutations of KIT or PDGFRA are critical in GISTs, because the aberrant versions not only are correlated with the specific cell morphology, histologic phenotype, metastasis, and prognosis, but also are the targets of therapy with imatinib and other agents.]. 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:18671247
;
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:NP231252.RAob6UGXmgIfmj9WPlFt0alQR1eYRVXJvgoV7RAgnSQy4130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:34:09+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" .
}