@prefix this: <
http://rdf.disgenet.org/resource/nanopub/NP1004261.RASj-VPbbudUrHRVMSmWnfU9t2eFIO3jXpokJaHHTW2tI
> .
@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/
> .
@prefix wi: <
http://purl.org/ontology/wi/core#
> .
@prefix prov: <
http://www.w3.org/ns/prov#
> .
@prefix pav: <
http://purl.org/pav/
> .
@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/resource/nanopub/
> .
@prefix dgn-gda: <
http://rdf.disgenet.org/resource/gda/
> .
@prefix dgn-void: <
http://rdf.disgenet.org/v4.0.0/void/
> .
dgn-np:NP1004261.RASj-VPbbudUrHRVMSmWnfU9t2eFIO3jXpokJaHHTW2tI130_head
{
this:
np:hasAssertion
dgn-np:NP1004261.RASj-VPbbudUrHRVMSmWnfU9t2eFIO3jXpokJaHHTW2tI130_assertion
;
np:hasProvenance
dgn-np:NP1004261.RASj-VPbbudUrHRVMSmWnfU9t2eFIO3jXpokJaHHTW2tI130_provenance
;
np:hasPublicationInfo
dgn-np:NP1004261.RASj-VPbbudUrHRVMSmWnfU9t2eFIO3jXpokJaHHTW2tI130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP1004261.RASj-VPbbudUrHRVMSmWnfU9t2eFIO3jXpokJaHHTW2tI130_assertion
a
np:Assertion
.
dgn-np:NP1004261.RASj-VPbbudUrHRVMSmWnfU9t2eFIO3jXpokJaHHTW2tI130_provenance
a
np:Provenance
.
dgn-np:NP1004261.RASj-VPbbudUrHRVMSmWnfU9t2eFIO3jXpokJaHHTW2tI130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP1004261.RASj-VPbbudUrHRVMSmWnfU9t2eFIO3jXpokJaHHTW2tI130_assertion
{
miriam-gene:5021
a
ncit:C16612
.
lld:C0033038
a
ncit:C7057
.
dgn-gda:DGN99f629d677d3d7a31aa8de97c742b114
sio:SIO_000628
miriam-gene:5021
,
lld:C0033038
;
a
sio:SIO_001122
.
}
dgn-np:NP1004261.RASj-VPbbudUrHRVMSmWnfU9t2eFIO3jXpokJaHHTW2tI130_provenance
{
dgn-np:NP1004261.RASj-VPbbudUrHRVMSmWnfU9t2eFIO3jXpokJaHHTW2tI130_assertion
dcterms:description
"[• We found a heterozygote effect on one SNP in the oxytocin receptor gene (rs75775), so that individuals heterozygous for this SNP had significantly elevated risk for premature ejaculation symptoms compared with carriers of either homozygote.]. 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:22882465
;
prov:wasDerivedFrom
dgn-void:befree-2016
;
prov:wasGeneratedBy
eco:ECO_0000203
.
dgn-void:befree-2016
pav:importedOn
"2016-02-19"^^
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:NP1004261.RASj-VPbbudUrHRVMSmWnfU9t2eFIO3jXpokJaHHTW2tI130_publicationInfo
{
this:
dcterms:created
"2016-05-13T12:49:21+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:disgenetv3.0rdf
;
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
"v4.0.0.0" .
dgn-void:disgenetv3.0rdf
pav:version
"v4.0.0" .
}