@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP274560.RAGJ9UH7arJySo331ADz8NcPSu_s1ZzFz9l3KNcvChAdI
> .
@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:NP274560.RAGJ9UH7arJySo331ADz8NcPSu_s1ZzFz9l3KNcvChAdI130_head
{
this:
np:hasAssertion
dgn-np:NP274560.RAGJ9UH7arJySo331ADz8NcPSu_s1ZzFz9l3KNcvChAdI130_assertion
;
np:hasProvenance
dgn-np:NP274560.RAGJ9UH7arJySo331ADz8NcPSu_s1ZzFz9l3KNcvChAdI130_provenance
;
np:hasPublicationInfo
dgn-np:NP274560.RAGJ9UH7arJySo331ADz8NcPSu_s1ZzFz9l3KNcvChAdI130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP274560.RAGJ9UH7arJySo331ADz8NcPSu_s1ZzFz9l3KNcvChAdI130_assertion
a
np:Assertion
.
dgn-np:NP274560.RAGJ9UH7arJySo331ADz8NcPSu_s1ZzFz9l3KNcvChAdI130_provenance
a
np:Provenance
.
dgn-np:NP274560.RAGJ9UH7arJySo331ADz8NcPSu_s1ZzFz9l3KNcvChAdI130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP274560.RAGJ9UH7arJySo331ADz8NcPSu_s1ZzFz9l3KNcvChAdI130_assertion
{
miriam-gene:6654
a
ncit:C16612
.
lld:C0006826
a
ncit:C7057
.
dgn-gda:DGN5592597d771c7b6ca274055fe7c38623
sio:SIO_000628
miriam-gene:6654
,
lld:C0006826
;
a
sio:SIO_001121
.
}
dgn-np:NP274560.RAGJ9UH7arJySo331ADz8NcPSu_s1ZzFz9l3KNcvChAdI130_provenance
{
dgn-np:NP274560.RAGJ9UH7arJySo331ADz8NcPSu_s1ZzFz9l3KNcvChAdI130_assertion
dcterms:description
"[Since autocrine regulation of HGF-Met is implicated in many forms of human cancer, we investigated whether the predisposition to develop ovarian cancer in women with hereditary ovarian cancer syndromes involves changes in the expression of HGF-Met by the tissue of origin of epithelial ovarian cancers, the ovarian surface epithelium (OSE).]. 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:11313876
;
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:NP274560.RAGJ9UH7arJySo331ADz8NcPSu_s1ZzFz9l3KNcvChAdI130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:34:34+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" .
}