@prefix dct: <
http://purl.org/dc/terms/
> .
@prefix orcid: <
http://orcid.org/
> .
@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP46234.RArwkenIKenhLbRG1oFcYRIZ93cfm_HBlG81j95GN7tWg
> .
@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 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:NP46234.RArwkenIKenhLbRG1oFcYRIZ93cfm_HBlG81j95GN7tWg130_head
{
this:
np:hasAssertion
dgn-np:NP46234.RArwkenIKenhLbRG1oFcYRIZ93cfm_HBlG81j95GN7tWg130_assertion
;
np:hasProvenance
dgn-np:NP46234.RArwkenIKenhLbRG1oFcYRIZ93cfm_HBlG81j95GN7tWg130_provenance
;
np:hasPublicationInfo
dgn-np:NP46234.RArwkenIKenhLbRG1oFcYRIZ93cfm_HBlG81j95GN7tWg130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP46234.RArwkenIKenhLbRG1oFcYRIZ93cfm_HBlG81j95GN7tWg130_assertion
a
np:Assertion
.
dgn-np:NP46234.RArwkenIKenhLbRG1oFcYRIZ93cfm_HBlG81j95GN7tWg130_provenance
a
np:Provenance
.
dgn-np:NP46234.RArwkenIKenhLbRG1oFcYRIZ93cfm_HBlG81j95GN7tWg130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP46234.RArwkenIKenhLbRG1oFcYRIZ93cfm_HBlG81j95GN7tWg130_assertion
{
miriam-gene:1586
a
ncit:C16612
.
lld:C2937421
a
ncit:C7057
.
dgn-gda:DGN512a4ee4291fcebe45473dbe3b79856a
sio:SIO_000628
miriam-gene:1586
,
lld:C2937421
;
a
sio:SIO_001122
.
}
dgn-np:NP46234.RArwkenIKenhLbRG1oFcYRIZ93cfm_HBlG81j95GN7tWg130_provenance
{
dgn-np:NP46234.RArwkenIKenhLbRG1oFcYRIZ93cfm_HBlG81j95GN7tWg130_assertion
dct:description
"[These results suggested that common variants of the CYP17 gene are associated with prostate enlargement and therefore may increase the risk of development of BPH in this population, while infrequent variants of the aromatase gene (CYP19) could be of a protective nature.]. 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:12370109
;
prov:wasDerivedFrom
dgn-void:gad-20130706
;
prov:wasGeneratedBy
eco:ECO_0000203
.
dgn-void:gad-20130706
pav:importedOn
"2013-07-06"^^
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:NP46234.RArwkenIKenhLbRG1oFcYRIZ93cfm_HBlG81j95GN7tWg130_publicationInfo
{
this:
dct:created
"2014-10-02T12:32:21+02:00"^^
xsd:dateTime
;
dct:rights
<
http://opendatacommons.org/licenses/odbl/1.0/
> ;
dct:rightsHolder
dgn-void:IBIGroup
;
dct:subject
sio:SIO_000983
;
prv:usedData
dgn-void:disgenetrdf
;
pav:authoredBy
orcid:0000-0001-5999-6269
,
orcid:0000-0002-7534-7661
,
orcid:0000-0002-9383-528X
,
orcid:0000-0003-0169-8159
,
orcid:0000-0003-1244-7654
;
pav:createdBy
orcid:0000-0003-0169-8159
;
pav:version
"v2.1.0.0" .
dgn-void:disgenetrdf
pav:version
"v2.1.0" .
}