@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP792974.RApFh0FfMWUpWtc7Jwujdq9xbl16R9R3vTZNpsqGVnH8U
> .
@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:NP792974.RApFh0FfMWUpWtc7Jwujdq9xbl16R9R3vTZNpsqGVnH8U130_head
{
this:
np:hasAssertion
dgn-np:NP792974.RApFh0FfMWUpWtc7Jwujdq9xbl16R9R3vTZNpsqGVnH8U130_assertion
;
np:hasProvenance
dgn-np:NP792974.RApFh0FfMWUpWtc7Jwujdq9xbl16R9R3vTZNpsqGVnH8U130_provenance
;
np:hasPublicationInfo
dgn-np:NP792974.RApFh0FfMWUpWtc7Jwujdq9xbl16R9R3vTZNpsqGVnH8U130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP792974.RApFh0FfMWUpWtc7Jwujdq9xbl16R9R3vTZNpsqGVnH8U130_assertion
a
np:Assertion
.
dgn-np:NP792974.RApFh0FfMWUpWtc7Jwujdq9xbl16R9R3vTZNpsqGVnH8U130_provenance
a
np:Provenance
.
dgn-np:NP792974.RApFh0FfMWUpWtc7Jwujdq9xbl16R9R3vTZNpsqGVnH8U130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP792974.RApFh0FfMWUpWtc7Jwujdq9xbl16R9R3vTZNpsqGVnH8U130_assertion
{
miriam-gene:1027
a
ncit:C16612
.
lld:C0238339
a
ncit:C7057
.
dgn-gda:DGN6dea077ea2bdda3456db9bd6bacf15ce
sio:SIO_000628
miriam-gene:1027
,
lld:C0238339
;
a
sio:SIO_001121
.
}
dgn-np:NP792974.RApFh0FfMWUpWtc7Jwujdq9xbl16R9R3vTZNpsqGVnH8U130_provenance
{
dgn-np:NP792974.RApFh0FfMWUpWtc7Jwujdq9xbl16R9R3vTZNpsqGVnH8U130_assertion
dcterms:description
"[In light of the evidence for linkage between the chromosomal location of the CDKN1B gene (12p13) and prostate cancer susceptibility in several hereditary prostate cancer (HPC) populations, we hypothesized that sequence variants of CDKN1B play a role in HPC.]. 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:15026335
;
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:NP792974.RApFh0FfMWUpWtc7Jwujdq9xbl16R9R3vTZNpsqGVnH8U130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:40:07+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" .
}