@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP511057.RAfWtbRAOiIEC5OYfminZZitlTrvm9n-JhStWqrrJ_NQg
> .
@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#
> .
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{
this:
np:hasAssertion
dgn-np:NP511057.RAfWtbRAOiIEC5OYfminZZitlTrvm9n-JhStWqrrJ_NQg130_assertion
;
np:hasProvenance
dgn-np:NP511057.RAfWtbRAOiIEC5OYfminZZitlTrvm9n-JhStWqrrJ_NQg130_provenance
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np:hasPublicationInfo
dgn-np:NP511057.RAfWtbRAOiIEC5OYfminZZitlTrvm9n-JhStWqrrJ_NQg130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP511057.RAfWtbRAOiIEC5OYfminZZitlTrvm9n-JhStWqrrJ_NQg130_assertion
a
np:Assertion
.
dgn-np:NP511057.RAfWtbRAOiIEC5OYfminZZitlTrvm9n-JhStWqrrJ_NQg130_provenance
a
np:Provenance
.
dgn-np:NP511057.RAfWtbRAOiIEC5OYfminZZitlTrvm9n-JhStWqrrJ_NQg130_publicationInfo
a
np:PublicationInfo
.
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{
miriam-gene:4985
a
ncit:C16612
.
lld:C0524662
a
ncit:C7057
.
dgn-gda:DGN889e585ed40bf45429d02805f15c4cec
sio:SIO_000628
miriam-gene:4985
,
lld:C0524662
;
a
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.
}
dgn-np:NP511057.RAfWtbRAOiIEC5OYfminZZitlTrvm9n-JhStWqrrJ_NQg130_provenance
{
dgn-np:NP511057.RAfWtbRAOiIEC5OYfminZZitlTrvm9n-JhStWqrrJ_NQg130_assertion
dcterms:description
"[Therefore, our data provide no support for the idea that variations in OPRM1, OPRD1, PENK and POMC are associated with alcohol dependence or general illicit drug dependence, but variations in PENK and POMC appear to be associated with the narrower phenotype of opioid dependence in these families.]. 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:17503481
;
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 .
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dgn-np:NP511057.RAfWtbRAOiIEC5OYfminZZitlTrvm9n-JhStWqrrJ_NQg130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:37:04+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
<
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> , <
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
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