@prefix dct: <
http://purl.org/dc/terms/
> .
@prefix orcid: <
http://orcid.org/
> .
@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP46232.RAqIhnrGkimrrnP_DG7C7Rdv6gq5iVdMYva6HmeSHHtd8
> .
@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:NP46232.RAqIhnrGkimrrnP_DG7C7Rdv6gq5iVdMYva6HmeSHHtd8130_head
{
this:
np:hasAssertion
dgn-np:NP46232.RAqIhnrGkimrrnP_DG7C7Rdv6gq5iVdMYva6HmeSHHtd8130_assertion
;
np:hasProvenance
dgn-np:NP46232.RAqIhnrGkimrrnP_DG7C7Rdv6gq5iVdMYva6HmeSHHtd8130_provenance
;
np:hasPublicationInfo
dgn-np:NP46232.RAqIhnrGkimrrnP_DG7C7Rdv6gq5iVdMYva6HmeSHHtd8130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP46232.RAqIhnrGkimrrnP_DG7C7Rdv6gq5iVdMYva6HmeSHHtd8130_assertion
a
np:Assertion
.
dgn-np:NP46232.RAqIhnrGkimrrnP_DG7C7Rdv6gq5iVdMYva6HmeSHHtd8130_provenance
a
np:Provenance
.
dgn-np:NP46232.RAqIhnrGkimrrnP_DG7C7Rdv6gq5iVdMYva6HmeSHHtd8130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP46232.RAqIhnrGkimrrnP_DG7C7Rdv6gq5iVdMYva6HmeSHHtd8130_assertion
{
miriam-gene:1586
a
ncit:C16612
.
lld:C0376358
a
ncit:C7057
.
dgn-gda:DGNad25da9f5efeb2d3080307fca1659819
sio:SIO_000628
miriam-gene:1586
,
lld:C0376358
;
a
sio:SIO_001122
.
}
dgn-np:NP46232.RAqIhnrGkimrrnP_DG7C7Rdv6gq5iVdMYva6HmeSHHtd8130_provenance
{
dgn-np:NP46232.RAqIhnrGkimrrnP_DG7C7Rdv6gq5iVdMYva6HmeSHHtd8130_assertion
dct:description
"[These observations have suggested that the CYP17 A2/A2, CYP1B1 Val/Val, and CYP2D6 genotypes may be associated with an altered risk of prostate cancer, while the CYP2D6 and SRD5A2 V89L polymorphism have no association with its risk in the North Indian 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:16716118
;
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:NP46232.RAqIhnrGkimrrnP_DG7C7Rdv6gq5iVdMYva6HmeSHHtd8130_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" .
}