@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP926756.RA1IcG93uPjJrIqQtsPJnIw1yr4L58D3o_jbc-YMTeMFg
> .
@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:NP926756.RA1IcG93uPjJrIqQtsPJnIw1yr4L58D3o_jbc-YMTeMFg130_head
{
this:
np:hasAssertion
dgn-np:NP926756.RA1IcG93uPjJrIqQtsPJnIw1yr4L58D3o_jbc-YMTeMFg130_assertion
;
np:hasProvenance
dgn-np:NP926756.RA1IcG93uPjJrIqQtsPJnIw1yr4L58D3o_jbc-YMTeMFg130_provenance
;
np:hasPublicationInfo
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;
a
np:Nanopublication
.
dgn-np:NP926756.RA1IcG93uPjJrIqQtsPJnIw1yr4L58D3o_jbc-YMTeMFg130_assertion
a
np:Assertion
.
dgn-np:NP926756.RA1IcG93uPjJrIqQtsPJnIw1yr4L58D3o_jbc-YMTeMFg130_provenance
a
np:Provenance
.
dgn-np:NP926756.RA1IcG93uPjJrIqQtsPJnIw1yr4L58D3o_jbc-YMTeMFg130_publicationInfo
a
np:PublicationInfo
.
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dgn-np:NP926756.RA1IcG93uPjJrIqQtsPJnIw1yr4L58D3o_jbc-YMTeMFg130_assertion
{
miriam-gene:5265
a
ncit:C16612
.
lld:C0036341
a
ncit:C7057
.
dgn-gda:DGN719cd1575f5125e72c84f44aff2312b3
sio:SIO_000628
miriam-gene:5265
,
lld:C0036341
;
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.
}
dgn-np:NP926756.RA1IcG93uPjJrIqQtsPJnIw1yr4L58D3o_jbc-YMTeMFg130_provenance
{
dgn-np:NP926756.RA1IcG93uPjJrIqQtsPJnIw1yr4L58D3o_jbc-YMTeMFg130_assertion
dcterms:description
"[The results demonstrate no association between CNR1 genotypes and schizophrenic disorders (P = 0.409), with these negative findings suggesting that, for Chinese populations, the (AAT)n triplet repeat in the promoter region of the CNR1 gene is not directly involved in the pathogenesis of schizophrenic disorders.]. 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:11204352
;
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:NP926756.RA1IcG93uPjJrIqQtsPJnIw1yr4L58D3o_jbc-YMTeMFg130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:41:28+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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> , <
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> , <
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> , <
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> ;
pav:createdBy
<
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> ;
pav:version
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dgn-void:disgenetrdf
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}