@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP178885.RAdPwVyrF15MuP-o0KTxOfK-K2nj2qqBwZZMQfaWUc98A
> .
@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:NP178885.RAdPwVyrF15MuP-o0KTxOfK-K2nj2qqBwZZMQfaWUc98A130_head
{
this:
np:hasAssertion
dgn-np:NP178885.RAdPwVyrF15MuP-o0KTxOfK-K2nj2qqBwZZMQfaWUc98A130_assertion
;
np:hasProvenance
dgn-np:NP178885.RAdPwVyrF15MuP-o0KTxOfK-K2nj2qqBwZZMQfaWUc98A130_provenance
;
np:hasPublicationInfo
dgn-np:NP178885.RAdPwVyrF15MuP-o0KTxOfK-K2nj2qqBwZZMQfaWUc98A130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP178885.RAdPwVyrF15MuP-o0KTxOfK-K2nj2qqBwZZMQfaWUc98A130_assertion
a
np:Assertion
.
dgn-np:NP178885.RAdPwVyrF15MuP-o0KTxOfK-K2nj2qqBwZZMQfaWUc98A130_provenance
a
np:Provenance
.
dgn-np:NP178885.RAdPwVyrF15MuP-o0KTxOfK-K2nj2qqBwZZMQfaWUc98A130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP178885.RAdPwVyrF15MuP-o0KTxOfK-K2nj2qqBwZZMQfaWUc98A130_assertion
{
miriam-gene:5627
a
ncit:C16612
.
lld:C0600139
a
ncit:C7057
.
dgn-gda:DGN755e075191fdab150c1d6820c72a5f20
sio:SIO_000628
miriam-gene:5627
,
lld:C0600139
;
a
sio:SIO_001121
.
}
dgn-np:NP178885.RAdPwVyrF15MuP-o0KTxOfK-K2nj2qqBwZZMQfaWUc98A130_provenance
{
dgn-np:NP178885.RAdPwVyrF15MuP-o0KTxOfK-K2nj2qqBwZZMQfaWUc98A130_assertion
dcterms:description
"[We therefore studied VDR gene polymorphisms, as detected by Apal and Taql restriction fragments, in multiethnic Brazilian men (165 patients and 200 controls) for association with prostate cancer risk and parameters of disease severity (serum PSA, Gleason score and tumor stage).]. 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:15503828
;
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:NP178885.RAdPwVyrF15MuP-o0KTxOfK-K2nj2qqBwZZMQfaWUc98A130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:33:37+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
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"v2.1.0" .
}