@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP641157.RAn_S6AAcnBZPyeoLm1xlWINFPPeWrSDa7_iDzrpCRJxQ
> .
@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:NP641157.RAn_S6AAcnBZPyeoLm1xlWINFPPeWrSDa7_iDzrpCRJxQ130_head
{
this:
np:hasAssertion
dgn-np:NP641157.RAn_S6AAcnBZPyeoLm1xlWINFPPeWrSDa7_iDzrpCRJxQ130_assertion
;
np:hasProvenance
dgn-np:NP641157.RAn_S6AAcnBZPyeoLm1xlWINFPPeWrSDa7_iDzrpCRJxQ130_provenance
;
np:hasPublicationInfo
dgn-np:NP641157.RAn_S6AAcnBZPyeoLm1xlWINFPPeWrSDa7_iDzrpCRJxQ130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP641157.RAn_S6AAcnBZPyeoLm1xlWINFPPeWrSDa7_iDzrpCRJxQ130_assertion
a
np:Assertion
.
dgn-np:NP641157.RAn_S6AAcnBZPyeoLm1xlWINFPPeWrSDa7_iDzrpCRJxQ130_provenance
a
np:Provenance
.
dgn-np:NP641157.RAn_S6AAcnBZPyeoLm1xlWINFPPeWrSDa7_iDzrpCRJxQ130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP641157.RAn_S6AAcnBZPyeoLm1xlWINFPPeWrSDa7_iDzrpCRJxQ130_assertion
{
miriam-gene:79017
a
ncit:C16612
.
lld:C1457883
a
ncit:C7057
.
dgn-gda:DGN198e0d95dcd179f82207e995357e76c4
sio:SIO_000628
miriam-gene:79017
,
lld:C1457883
;
a
sio:SIO_001121
.
}
dgn-np:NP641157.RAn_S6AAcnBZPyeoLm1xlWINFPPeWrSDa7_iDzrpCRJxQ130_provenance
{
dgn-np:NP641157.RAn_S6AAcnBZPyeoLm1xlWINFPPeWrSDa7_iDzrpCRJxQ130_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:NP641157.RAn_S6AAcnBZPyeoLm1xlWINFPPeWrSDa7_iDzrpCRJxQ130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:38:26+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" .
}