@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP47325.RA_EebPnuMqHM3m_aXVy-S1d0CpqaGjzTa-sWJpaYcmaY
> .
@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:NP47325.RA_EebPnuMqHM3m_aXVy-S1d0CpqaGjzTa-sWJpaYcmaY130_head
{
this:
np:hasAssertion
dgn-np:NP47325.RA_EebPnuMqHM3m_aXVy-S1d0CpqaGjzTa-sWJpaYcmaY130_assertion
;
np:hasProvenance
dgn-np:NP47325.RA_EebPnuMqHM3m_aXVy-S1d0CpqaGjzTa-sWJpaYcmaY130_provenance
;
np:hasPublicationInfo
dgn-np:NP47325.RA_EebPnuMqHM3m_aXVy-S1d0CpqaGjzTa-sWJpaYcmaY130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP47325.RA_EebPnuMqHM3m_aXVy-S1d0CpqaGjzTa-sWJpaYcmaY130_assertion
a
np:Assertion
.
dgn-np:NP47325.RA_EebPnuMqHM3m_aXVy-S1d0CpqaGjzTa-sWJpaYcmaY130_provenance
a
np:Provenance
.
dgn-np:NP47325.RA_EebPnuMqHM3m_aXVy-S1d0CpqaGjzTa-sWJpaYcmaY130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP47325.RA_EebPnuMqHM3m_aXVy-S1d0CpqaGjzTa-sWJpaYcmaY130_assertion
{
miriam-gene:595
a
ncit:C16612
.
lld:C0376358
a
ncit:C7057
.
dgn-gda:DGN112935e6da5657311fc89e978cf457d4
sio:SIO_000628
miriam-gene:595
,
lld:C0376358
;
a
sio:SIO_001122
.
}
dgn-np:NP47325.RA_EebPnuMqHM3m_aXVy-S1d0CpqaGjzTa-sWJpaYcmaY130_provenance
{
dgn-np:NP47325.RA_EebPnuMqHM3m_aXVy-S1d0CpqaGjzTa-sWJpaYcmaY130_assertion
dcterms:description
"[The A allele of the CCND1 A870G polymorphism was recessively associated with susceptibility to PCa and BPH in a Japanese population, giving a 2-fold increased risk of PCa and BPH in men with the AA genotype compared to those with the GG genotype. Although the risk of PCa associated with the AA genotype appeared to contribute especially to men aged 73 years or younger and the A allele may be associated with disease status of PCa, these conjectures require validation in future studies on a larger number of subjects.]. 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:12455063
;
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:NP47325.RA_EebPnuMqHM3m_aXVy-S1d0CpqaGjzTa-sWJpaYcmaY130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:32:21+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" .
}