@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP711889.RAw8egwNFVLoKhAHY3daxXi7h-aFRf_tcuSV7myrd8lQM
> .
@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:NP711889.RAw8egwNFVLoKhAHY3daxXi7h-aFRf_tcuSV7myrd8lQM130_head
{
this:
np:hasAssertion
dgn-np:NP711889.RAw8egwNFVLoKhAHY3daxXi7h-aFRf_tcuSV7myrd8lQM130_assertion
;
np:hasProvenance
dgn-np:NP711889.RAw8egwNFVLoKhAHY3daxXi7h-aFRf_tcuSV7myrd8lQM130_provenance
;
np:hasPublicationInfo
dgn-np:NP711889.RAw8egwNFVLoKhAHY3daxXi7h-aFRf_tcuSV7myrd8lQM130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP711889.RAw8egwNFVLoKhAHY3daxXi7h-aFRf_tcuSV7myrd8lQM130_assertion
a
np:Assertion
.
dgn-np:NP711889.RAw8egwNFVLoKhAHY3daxXi7h-aFRf_tcuSV7myrd8lQM130_provenance
a
np:Provenance
.
dgn-np:NP711889.RAw8egwNFVLoKhAHY3daxXi7h-aFRf_tcuSV7myrd8lQM130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP711889.RAw8egwNFVLoKhAHY3daxXi7h-aFRf_tcuSV7myrd8lQM130_assertion
{
miriam-gene:5156
a
ncit:C16612
.
lld:C2939420
a
ncit:C7057
.
dgn-gda:DGNba18dcf73ea07395027d497e1cd99236
sio:SIO_000628
miriam-gene:5156
,
lld:C2939420
;
a
sio:SIO_001121
.
}
dgn-np:NP711889.RAw8egwNFVLoKhAHY3daxXi7h-aFRf_tcuSV7myrd8lQM130_provenance
{
dgn-np:NP711889.RAw8egwNFVLoKhAHY3daxXi7h-aFRf_tcuSV7myrd8lQM130_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:NP711889.RAw8egwNFVLoKhAHY3daxXi7h-aFRf_tcuSV7myrd8lQM130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:39:12+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" .
}