@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP827441.RA_dd3V2t382WU8dRy6XtfB5HHDaNyJkFgpvwwHNK_p14
> .
@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:NP827441.RA_dd3V2t382WU8dRy6XtfB5HHDaNyJkFgpvwwHNK_p14130_head
{
this:
np:hasAssertion
dgn-np:NP827441.RA_dd3V2t382WU8dRy6XtfB5HHDaNyJkFgpvwwHNK_p14130_assertion
;
np:hasProvenance
dgn-np:NP827441.RA_dd3V2t382WU8dRy6XtfB5HHDaNyJkFgpvwwHNK_p14130_provenance
;
np:hasPublicationInfo
dgn-np:NP827441.RA_dd3V2t382WU8dRy6XtfB5HHDaNyJkFgpvwwHNK_p14130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP827441.RA_dd3V2t382WU8dRy6XtfB5HHDaNyJkFgpvwwHNK_p14130_assertion
a
np:Assertion
.
dgn-np:NP827441.RA_dd3V2t382WU8dRy6XtfB5HHDaNyJkFgpvwwHNK_p14130_provenance
a
np:Provenance
.
dgn-np:NP827441.RA_dd3V2t382WU8dRy6XtfB5HHDaNyJkFgpvwwHNK_p14130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP827441.RA_dd3V2t382WU8dRy6XtfB5HHDaNyJkFgpvwwHNK_p14130_assertion
{
miriam-gene:6928
a
ncit:C16612
.
lld:C0006826
a
ncit:C7057
.
dgn-gda:DGNdd825a4cafa0fa3778c6818ddfc9c7c1
sio:SIO_000628
miriam-gene:6928
,
lld:C0006826
;
a
sio:SIO_001121
.
}
dgn-np:NP827441.RA_dd3V2t382WU8dRy6XtfB5HHDaNyJkFgpvwwHNK_p14130_provenance
{
dgn-np:NP827441.RA_dd3V2t382WU8dRy6XtfB5HHDaNyJkFgpvwwHNK_p14130_assertion
dcterms:description
"[To fine-map common genetic variation in this region, we genotyped 79 single nucleotide polymorphisms (SNPs) in the 17q12 region harboring HNF1B in 10 272 prostate cancer cases and 9123 controls of European ancestry from 10 case-control studies as part of the Cancer Genetic Markers of Susceptibility (CGEMS) initiative.]. 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:21576123
;
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:NP827441.RA_dd3V2t382WU8dRy6XtfB5HHDaNyJkFgpvwwHNK_p14130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:40:26+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" .
}