@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP315714.RApEAig67FxL4UrCGziYbo-u8usMhtUD16FFx29gXodk8
> .
@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:NP315714.RApEAig67FxL4UrCGziYbo-u8usMhtUD16FFx29gXodk8130_head
{
this:
np:hasAssertion
dgn-np:NP315714.RApEAig67FxL4UrCGziYbo-u8usMhtUD16FFx29gXodk8130_assertion
;
np:hasProvenance
dgn-np:NP315714.RApEAig67FxL4UrCGziYbo-u8usMhtUD16FFx29gXodk8130_provenance
;
np:hasPublicationInfo
dgn-np:NP315714.RApEAig67FxL4UrCGziYbo-u8usMhtUD16FFx29gXodk8130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP315714.RApEAig67FxL4UrCGziYbo-u8usMhtUD16FFx29gXodk8130_assertion
a
np:Assertion
.
dgn-np:NP315714.RApEAig67FxL4UrCGziYbo-u8usMhtUD16FFx29gXodk8130_provenance
a
np:Provenance
.
dgn-np:NP315714.RApEAig67FxL4UrCGziYbo-u8usMhtUD16FFx29gXodk8130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP315714.RApEAig67FxL4UrCGziYbo-u8usMhtUD16FFx29gXodk8130_assertion
{
miriam-gene:373156
a
ncit:C16612
.
lld:C1458156
a
ncit:C7057
.
dgn-gda:DGN0ae78f6e0dc901821009526ba2d48b1b
sio:SIO_000628
miriam-gene:373156
,
lld:C1458156
;
a
sio:SIO_001121
.
}
dgn-np:NP315714.RApEAig67FxL4UrCGziYbo-u8usMhtUD16FFx29gXodk8130_provenance
{
dgn-np:NP315714.RApEAig67FxL4UrCGziYbo-u8usMhtUD16FFx29gXodk8130_assertion
dcterms:description
"[Although the GSTM1 null genotype has been shown to increase prostate cancer mortality in Caucasians, potential associations between GST polymorphisms and prostate cancer biochemical recurrence (BCR) have not been well studied, particularly in African-Americans.]. 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:19568698
;
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:NP315714.RApEAig67FxL4UrCGziYbo-u8usMhtUD16FFx29gXodk8130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:35:01+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" .
}