@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP192043.RA7LUOEkvsoOezOGa-lyC0ntMG2qij1y6ZSY0SMqpeM3I
> .
@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#
> .
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{
this:
np:hasAssertion
dgn-np:NP192043.RA7LUOEkvsoOezOGa-lyC0ntMG2qij1y6ZSY0SMqpeM3I130_assertion
;
np:hasProvenance
dgn-np:NP192043.RA7LUOEkvsoOezOGa-lyC0ntMG2qij1y6ZSY0SMqpeM3I130_provenance
;
np:hasPublicationInfo
dgn-np:NP192043.RA7LUOEkvsoOezOGa-lyC0ntMG2qij1y6ZSY0SMqpeM3I130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP192043.RA7LUOEkvsoOezOGa-lyC0ntMG2qij1y6ZSY0SMqpeM3I130_assertion
a
np:Assertion
.
dgn-np:NP192043.RA7LUOEkvsoOezOGa-lyC0ntMG2qij1y6ZSY0SMqpeM3I130_provenance
a
np:Provenance
.
dgn-np:NP192043.RA7LUOEkvsoOezOGa-lyC0ntMG2qij1y6ZSY0SMqpeM3I130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP192043.RA7LUOEkvsoOezOGa-lyC0ntMG2qij1y6ZSY0SMqpeM3I130_assertion
{
miriam-gene:2272
a
ncit:C16612
.
lld:C0677886
a
ncit:C7057
.
dgn-gda:DGNd6fda9e26c46ee5fe03f485de03f4f05
sio:SIO_000628
miriam-gene:2272
,
lld:C0677886
;
a
sio:SIO_001121
.
}
dgn-np:NP192043.RA7LUOEkvsoOezOGa-lyC0ntMG2qij1y6ZSY0SMqpeM3I130_provenance
{
dgn-np:NP192043.RA7LUOEkvsoOezOGa-lyC0ntMG2qij1y6ZSY0SMqpeM3I130_assertion
dcterms:description
"[The present data suggest that inactivation of the FHIT gene by loss of expression is one of the important molecular events associated with the genesis of ovarian carcinoma, especially of high-grade serous carcinoma.]. 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:11461085
;
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:NP192043.RA7LUOEkvsoOezOGa-lyC0ntMG2qij1y6ZSY0SMqpeM3I130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:33:45+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
<
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> , <
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" .
}