@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP785676.RA8zfRzZ6pvnGNtKEmhmQfXmPHSi27P9E8aQPBMP41-kg
> .
@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:NP785676.RA8zfRzZ6pvnGNtKEmhmQfXmPHSi27P9E8aQPBMP41-kg130_head
{
this:
np:hasAssertion
dgn-np:NP785676.RA8zfRzZ6pvnGNtKEmhmQfXmPHSi27P9E8aQPBMP41-kg130_assertion
;
np:hasProvenance
dgn-np:NP785676.RA8zfRzZ6pvnGNtKEmhmQfXmPHSi27P9E8aQPBMP41-kg130_provenance
;
np:hasPublicationInfo
dgn-np:NP785676.RA8zfRzZ6pvnGNtKEmhmQfXmPHSi27P9E8aQPBMP41-kg130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP785676.RA8zfRzZ6pvnGNtKEmhmQfXmPHSi27P9E8aQPBMP41-kg130_assertion
a
np:Assertion
.
dgn-np:NP785676.RA8zfRzZ6pvnGNtKEmhmQfXmPHSi27P9E8aQPBMP41-kg130_provenance
a
np:Provenance
.
dgn-np:NP785676.RA8zfRzZ6pvnGNtKEmhmQfXmPHSi27P9E8aQPBMP41-kg130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP785676.RA8zfRzZ6pvnGNtKEmhmQfXmPHSi27P9E8aQPBMP41-kg130_assertion
{
miriam-gene:9730
a
ncit:C16612
.
lld:C0085281
a
ncit:C7057
.
dgn-gda:DGNcf4c17e4485cee4d80148fbc7e0442cf
sio:SIO_000628
miriam-gene:9730
,
lld:C0085281
;
a
sio:SIO_001121
.
}
dgn-np:NP785676.RA8zfRzZ6pvnGNtKEmhmQfXmPHSi27P9E8aQPBMP41-kg130_provenance
{
dgn-np:NP785676.RA8zfRzZ6pvnGNtKEmhmQfXmPHSi27P9E8aQPBMP41-kg130_assertion
dcterms:description
"[The TaqIA single-nucleotide polymorphism (SNP), which is the most widely studied genetic polymorphism in addictions, is located at the gene that encodes the RIP kinase ANKK1 near the gene for dopamine receptor D2.]. 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:20845092
;
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:NP785676.RA8zfRzZ6pvnGNtKEmhmQfXmPHSi27P9E8aQPBMP41-kg130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:39:56+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" .
}