@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP223692.RAdWaLpS3afiSqTBsEEPtQ7IVnxylZ1o-94RqRUOsU3OI
> .
@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:NP223692.RAdWaLpS3afiSqTBsEEPtQ7IVnxylZ1o-94RqRUOsU3OI130_head
{
this:
np:hasAssertion
dgn-np:NP223692.RAdWaLpS3afiSqTBsEEPtQ7IVnxylZ1o-94RqRUOsU3OI130_assertion
;
np:hasProvenance
dgn-np:NP223692.RAdWaLpS3afiSqTBsEEPtQ7IVnxylZ1o-94RqRUOsU3OI130_provenance
;
np:hasPublicationInfo
dgn-np:NP223692.RAdWaLpS3afiSqTBsEEPtQ7IVnxylZ1o-94RqRUOsU3OI130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP223692.RAdWaLpS3afiSqTBsEEPtQ7IVnxylZ1o-94RqRUOsU3OI130_assertion
a
np:Assertion
.
dgn-np:NP223692.RAdWaLpS3afiSqTBsEEPtQ7IVnxylZ1o-94RqRUOsU3OI130_provenance
a
np:Provenance
.
dgn-np:NP223692.RAdWaLpS3afiSqTBsEEPtQ7IVnxylZ1o-94RqRUOsU3OI130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP223692.RAdWaLpS3afiSqTBsEEPtQ7IVnxylZ1o-94RqRUOsU3OI130_assertion
{
miriam-gene:4988
a
ncit:C16612
.
lld:C0038580
a
ncit:C7057
.
dgn-gda:DGN9b4ecfa713dbee2cfcaa4aca2c448624
sio:SIO_000628
miriam-gene:4988
,
lld:C0038580
;
a
sio:SIO_001121
.
}
dgn-np:NP223692.RAdWaLpS3afiSqTBsEEPtQ7IVnxylZ1o-94RqRUOsU3OI130_provenance
{
dgn-np:NP223692.RAdWaLpS3afiSqTBsEEPtQ7IVnxylZ1o-94RqRUOsU3OI130_assertion
dcterms:description
"[Previous studies of the association of the C17T polymorphism of the mu opiate receptor gene with substance dependence compared cases with substance dependence to controls and usually found no significant association.]. 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:21070507
;
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:NP223692.RAdWaLpS3afiSqTBsEEPtQ7IVnxylZ1o-94RqRUOsU3OI130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:34:04+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
<
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" .
}