@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP593158.RAeHGSGJK68Q14nBTumf4_VGvzRsPWljlIg7SaE_ovMNY
> .
@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:NP593158.RAeHGSGJK68Q14nBTumf4_VGvzRsPWljlIg7SaE_ovMNY130_head
{
this:
np:hasAssertion
dgn-np:NP593158.RAeHGSGJK68Q14nBTumf4_VGvzRsPWljlIg7SaE_ovMNY130_assertion
;
np:hasProvenance
dgn-np:NP593158.RAeHGSGJK68Q14nBTumf4_VGvzRsPWljlIg7SaE_ovMNY130_provenance
;
np:hasPublicationInfo
dgn-np:NP593158.RAeHGSGJK68Q14nBTumf4_VGvzRsPWljlIg7SaE_ovMNY130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP593158.RAeHGSGJK68Q14nBTumf4_VGvzRsPWljlIg7SaE_ovMNY130_assertion
a
np:Assertion
.
dgn-np:NP593158.RAeHGSGJK68Q14nBTumf4_VGvzRsPWljlIg7SaE_ovMNY130_provenance
a
np:Provenance
.
dgn-np:NP593158.RAeHGSGJK68Q14nBTumf4_VGvzRsPWljlIg7SaE_ovMNY130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP593158.RAeHGSGJK68Q14nBTumf4_VGvzRsPWljlIg7SaE_ovMNY130_assertion
{
miriam-gene:81539
a
ncit:C16612
.
lld:C0600139
a
ncit:C7057
.
dgn-gda:DGN88599acc48c0fbc343a7dad57c151b3f
sio:SIO_000628
miriam-gene:81539
,
lld:C0600139
;
a
sio:SIO_001121
.
}
dgn-np:NP593158.RAeHGSGJK68Q14nBTumf4_VGvzRsPWljlIg7SaE_ovMNY130_provenance
{
dgn-np:NP593158.RAeHGSGJK68Q14nBTumf4_VGvzRsPWljlIg7SaE_ovMNY130_assertion
dcterms:description
"[These data demonstrate that the NAT2 slow acetylator genotype plays an important role in determining the risk of developing prostate cancer in Japanese men and is also associated with more clinically advanced and pathologically aggressive disease.]. 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:12622714
;
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:NP593158.RAeHGSGJK68Q14nBTumf4_VGvzRsPWljlIg7SaE_ovMNY130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:37:56+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" .
}