@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP805317.RA2AYsW8GRSZOVGnW_g_d_2DYWHTyt8IqD0jb4UywzMGs
> .
@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:NP805317.RA2AYsW8GRSZOVGnW_g_d_2DYWHTyt8IqD0jb4UywzMGs130_head
{
this:
np:hasAssertion
dgn-np:NP805317.RA2AYsW8GRSZOVGnW_g_d_2DYWHTyt8IqD0jb4UywzMGs130_assertion
;
np:hasProvenance
dgn-np:NP805317.RA2AYsW8GRSZOVGnW_g_d_2DYWHTyt8IqD0jb4UywzMGs130_provenance
;
np:hasPublicationInfo
dgn-np:NP805317.RA2AYsW8GRSZOVGnW_g_d_2DYWHTyt8IqD0jb4UywzMGs130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP805317.RA2AYsW8GRSZOVGnW_g_d_2DYWHTyt8IqD0jb4UywzMGs130_assertion
a
np:Assertion
.
dgn-np:NP805317.RA2AYsW8GRSZOVGnW_g_d_2DYWHTyt8IqD0jb4UywzMGs130_provenance
a
np:Provenance
.
dgn-np:NP805317.RA2AYsW8GRSZOVGnW_g_d_2DYWHTyt8IqD0jb4UywzMGs130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP805317.RA2AYsW8GRSZOVGnW_g_d_2DYWHTyt8IqD0jb4UywzMGs130_assertion
{
miriam-gene:6716
a
ncit:C16612
.
lld:C1457883
a
ncit:C7057
.
dgn-gda:DGN753340fcfae6606d3e8907fe9c451121
sio:SIO_000628
miriam-gene:6716
,
lld:C1457883
;
a
sio:SIO_001121
.
}
dgn-np:NP805317.RA2AYsW8GRSZOVGnW_g_d_2DYWHTyt8IqD0jb4UywzMGs130_provenance
{
dgn-np:NP805317.RA2AYsW8GRSZOVGnW_g_d_2DYWHTyt8IqD0jb4UywzMGs130_assertion
dcterms:description
"[The prostate is an androgen-regulated organ and polymorphisms in genes involved in testosterone synthesis, in particular, SRD5A2 (A49T and V89L variants), CYP17 (MspAI variant), and the AR (CAG, GGC repeats), represent candidate risk factors for prostate cancer incidence and aggressiveness.]. 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:14991867
;
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:NP805317.RA2AYsW8GRSZOVGnW_g_d_2DYWHTyt8IqD0jb4UywzMGs130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:40:14+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" .
}