@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP301607.RApzC5VgsSogtzCDomgYKxMcrm-v-x348mTBzVaDiDPIA
> .
@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:NP301607.RApzC5VgsSogtzCDomgYKxMcrm-v-x348mTBzVaDiDPIA130_head
{
this:
np:hasAssertion
dgn-np:NP301607.RApzC5VgsSogtzCDomgYKxMcrm-v-x348mTBzVaDiDPIA130_assertion
;
np:hasProvenance
dgn-np:NP301607.RApzC5VgsSogtzCDomgYKxMcrm-v-x348mTBzVaDiDPIA130_provenance
;
np:hasPublicationInfo
dgn-np:NP301607.RApzC5VgsSogtzCDomgYKxMcrm-v-x348mTBzVaDiDPIA130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP301607.RApzC5VgsSogtzCDomgYKxMcrm-v-x348mTBzVaDiDPIA130_assertion
a
np:Assertion
.
dgn-np:NP301607.RApzC5VgsSogtzCDomgYKxMcrm-v-x348mTBzVaDiDPIA130_provenance
a
np:Provenance
.
dgn-np:NP301607.RApzC5VgsSogtzCDomgYKxMcrm-v-x348mTBzVaDiDPIA130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP301607.RApzC5VgsSogtzCDomgYKxMcrm-v-x348mTBzVaDiDPIA130_assertion
{
miriam-gene:1588
a
ncit:C16612
.
lld:C0600139
a
ncit:C7057
.
dgn-gda:DGN2293f0121743c456b505ba387c909471
sio:SIO_000628
miriam-gene:1588
,
lld:C0600139
;
a
sio:SIO_001121
.
}
dgn-np:NP301607.RApzC5VgsSogtzCDomgYKxMcrm-v-x348mTBzVaDiDPIA130_provenance
{
dgn-np:NP301607.RApzC5VgsSogtzCDomgYKxMcrm-v-x348mTBzVaDiDPIA130_assertion
dcterms:description
"[The purpose of this study was to determine whether polymorphisms in the CAG repeat in exon 1 of the androgen receptor (AR), two intronic restriction sites in the estrogen receptor (ESR1 XbaI and ESR1 PvuII), and an Arg264Cy5 substitution in the aromatase gene (CYP19) contribute to prostate cancer risk.]. 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:11595700
;
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:NP301607.RApzC5VgsSogtzCDomgYKxMcrm-v-x348mTBzVaDiDPIA130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:34:51+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" .
}