@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP825236.RAHmXY_VTxhG2gAMwq1GzBz90ljOMzX2zcvL8HMX9IT9Q
> .
@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:NP825236.RAHmXY_VTxhG2gAMwq1GzBz90ljOMzX2zcvL8HMX9IT9Q130_head
{
this:
np:hasAssertion
dgn-np:NP825236.RAHmXY_VTxhG2gAMwq1GzBz90ljOMzX2zcvL8HMX9IT9Q130_assertion
;
np:hasProvenance
dgn-np:NP825236.RAHmXY_VTxhG2gAMwq1GzBz90ljOMzX2zcvL8HMX9IT9Q130_provenance
;
np:hasPublicationInfo
dgn-np:NP825236.RAHmXY_VTxhG2gAMwq1GzBz90ljOMzX2zcvL8HMX9IT9Q130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP825236.RAHmXY_VTxhG2gAMwq1GzBz90ljOMzX2zcvL8HMX9IT9Q130_assertion
a
np:Assertion
.
dgn-np:NP825236.RAHmXY_VTxhG2gAMwq1GzBz90ljOMzX2zcvL8HMX9IT9Q130_provenance
a
np:Provenance
.
dgn-np:NP825236.RAHmXY_VTxhG2gAMwq1GzBz90ljOMzX2zcvL8HMX9IT9Q130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP825236.RAHmXY_VTxhG2gAMwq1GzBz90ljOMzX2zcvL8HMX9IT9Q130_assertion
{
miriam-gene:1268
a
ncit:C16612
.
lld:C0030567
a
ncit:C7057
.
dgn-gda:DGN47aecc1f2eeee000c788ce994ce1e253
sio:SIO_000628
miriam-gene:1268
,
lld:C0030567
;
a
sio:SIO_001121
.
}
dgn-np:NP825236.RAHmXY_VTxhG2gAMwq1GzBz90ljOMzX2zcvL8HMX9IT9Q130_provenance
{
dgn-np:NP825236.RAHmXY_VTxhG2gAMwq1GzBz90ljOMzX2zcvL8HMX9IT9Q130_assertion
dcterms:description
"[The cloning of the human cannabinoid receptor (CNR1) gene facilitates molecular genetic studies in disorders like Gilles de la Tourette syndrome (GTS), obsessive compulsive disorder (OCD), Parkinsons disease, Alzheimers disease or other neuro psychiatric or neurological diseases, which may be predisposed or influenced by mutations or variants in the CNR1 gene.]. 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:10441206
;
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:NP825236.RAHmXY_VTxhG2gAMwq1GzBz90ljOMzX2zcvL8HMX9IT9Q130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:40:25+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" .
}