@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP313028.RA28vvSBHW_LJ6vn33z4UZ24qIIWmWzEOm5uVIo-PDc3I
> .
@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:NP313028.RA28vvSBHW_LJ6vn33z4UZ24qIIWmWzEOm5uVIo-PDc3I130_head
{
this:
np:hasAssertion
dgn-np:NP313028.RA28vvSBHW_LJ6vn33z4UZ24qIIWmWzEOm5uVIo-PDc3I130_assertion
;
np:hasProvenance
dgn-np:NP313028.RA28vvSBHW_LJ6vn33z4UZ24qIIWmWzEOm5uVIo-PDc3I130_provenance
;
np:hasPublicationInfo
dgn-np:NP313028.RA28vvSBHW_LJ6vn33z4UZ24qIIWmWzEOm5uVIo-PDc3I130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP313028.RA28vvSBHW_LJ6vn33z4UZ24qIIWmWzEOm5uVIo-PDc3I130_assertion
a
np:Assertion
.
dgn-np:NP313028.RA28vvSBHW_LJ6vn33z4UZ24qIIWmWzEOm5uVIo-PDc3I130_provenance
a
np:Provenance
.
dgn-np:NP313028.RA28vvSBHW_LJ6vn33z4UZ24qIIWmWzEOm5uVIo-PDc3I130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP313028.RA28vvSBHW_LJ6vn33z4UZ24qIIWmWzEOm5uVIo-PDc3I130_assertion
{
miriam-gene:1815
a
ncit:C16612
.
lld:C0013146
a
ncit:C7057
.
dgn-gda:DGNf471210cd320e5f79d20d9239e5a7070
sio:SIO_000628
miriam-gene:1815
,
lld:C0013146
;
a
sio:SIO_001121
.
}
dgn-np:NP313028.RA28vvSBHW_LJ6vn33z4UZ24qIIWmWzEOm5uVIo-PDc3I130_provenance
{
dgn-np:NP313028.RA28vvSBHW_LJ6vn33z4UZ24qIIWmWzEOm5uVIo-PDc3I130_assertion
dcterms:description
"[Genetic variability at the DRD4 gene is involved in the predisposition to episodic MO but not to DA, while liability to CDHDA may involve genetic variability at the DAT gene in comparison with episodic MO.]. 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:16930369
;
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:NP313028.RA28vvSBHW_LJ6vn33z4UZ24qIIWmWzEOm5uVIo-PDc3I130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:34:59+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" .
}