@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP684134.RA0zpumO8OFox4db8OqyqWo2rpJ9hXSerI0zgpP2GEHG0
> .
@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:NP684134.RA0zpumO8OFox4db8OqyqWo2rpJ9hXSerI0zgpP2GEHG0130_head
{
this:
np:hasAssertion
dgn-np:NP684134.RA0zpumO8OFox4db8OqyqWo2rpJ9hXSerI0zgpP2GEHG0130_assertion
;
np:hasProvenance
dgn-np:NP684134.RA0zpumO8OFox4db8OqyqWo2rpJ9hXSerI0zgpP2GEHG0130_provenance
;
np:hasPublicationInfo
dgn-np:NP684134.RA0zpumO8OFox4db8OqyqWo2rpJ9hXSerI0zgpP2GEHG0130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP684134.RA0zpumO8OFox4db8OqyqWo2rpJ9hXSerI0zgpP2GEHG0130_assertion
a
np:Assertion
.
dgn-np:NP684134.RA0zpumO8OFox4db8OqyqWo2rpJ9hXSerI0zgpP2GEHG0130_provenance
a
np:Provenance
.
dgn-np:NP684134.RA0zpumO8OFox4db8OqyqWo2rpJ9hXSerI0zgpP2GEHG0130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP684134.RA0zpumO8OFox4db8OqyqWo2rpJ9hXSerI0zgpP2GEHG0130_assertion
{
miriam-gene:5831
a
ncit:C16612
.
lld:C1704272
a
ncit:C7057
.
dgn-gda:DGNbb57fac1752cbeb8692af58685bd9970
sio:SIO_000628
miriam-gene:5831
,
lld:C1704272
;
a
sio:SIO_001121
.
}
dgn-np:NP684134.RA0zpumO8OFox4db8OqyqWo2rpJ9hXSerI0zgpP2GEHG0130_provenance
{
dgn-np:NP684134.RA0zpumO8OFox4db8OqyqWo2rpJ9hXSerI0zgpP2GEHG0130_assertion
dcterms:description
"[These four variants, plus two other variants (PRO3 and INDEL1) that have been linked to prostate cancer risk in the previous studies, were typed for all study subjects, which included 130 prostate cancer cases, 130 patients with benign prostatic hyperplasia and 150 controls randomly selected from the population.]. 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:17768178
;
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:NP684134.RA0zpumO8OFox4db8OqyqWo2rpJ9hXSerI0zgpP2GEHG0130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:38:56+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" .
}