@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP491745.RANDZsft0sd5bHzsR5gNu9QJawbwEfUn9kAKcmxBhVdvU
> .
@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:NP491745.RANDZsft0sd5bHzsR5gNu9QJawbwEfUn9kAKcmxBhVdvU130_head
{
this:
np:hasAssertion
dgn-np:NP491745.RANDZsft0sd5bHzsR5gNu9QJawbwEfUn9kAKcmxBhVdvU130_assertion
;
np:hasProvenance
dgn-np:NP491745.RANDZsft0sd5bHzsR5gNu9QJawbwEfUn9kAKcmxBhVdvU130_provenance
;
np:hasPublicationInfo
dgn-np:NP491745.RANDZsft0sd5bHzsR5gNu9QJawbwEfUn9kAKcmxBhVdvU130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP491745.RANDZsft0sd5bHzsR5gNu9QJawbwEfUn9kAKcmxBhVdvU130_assertion
a
np:Assertion
.
dgn-np:NP491745.RANDZsft0sd5bHzsR5gNu9QJawbwEfUn9kAKcmxBhVdvU130_provenance
a
np:Provenance
.
dgn-np:NP491745.RANDZsft0sd5bHzsR5gNu9QJawbwEfUn9kAKcmxBhVdvU130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP491745.RANDZsft0sd5bHzsR5gNu9QJawbwEfUn9kAKcmxBhVdvU130_assertion
{
miriam-gene:1588
a
ncit:C16612
.
lld:C0600139
a
ncit:C7057
.
dgn-gda:DGNb7bf5a151015356821b6bc3b13e60a64
sio:SIO_000628
miriam-gene:1588
,
lld:C0600139
;
a
sio:SIO_001121
.
}
dgn-np:NP491745.RANDZsft0sd5bHzsR5gNu9QJawbwEfUn9kAKcmxBhVdvU130_provenance
{
dgn-np:NP491745.RANDZsft0sd5bHzsR5gNu9QJawbwEfUn9kAKcmxBhVdvU130_assertion
dcterms:description
"[Here we report on findings from a comprehensive study of genetic variation at the CYP19A1 locus in relation to prostate cancer risk and to circulating steroid hormone concentrations in men by the Breast and Prostate Cancer Cohort Consortium (BPC3), a large collaborative prospective study.]. 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:19789370
;
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:NP491745.RANDZsft0sd5bHzsR5gNu9QJawbwEfUn9kAKcmxBhVdvU130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:36:53+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" .
}