@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP64073.RASa6f1RPt7un_1AhRYe6TAsTgBD-hEr9m1ZfLuc1eFkg
> .
@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:NP64073.RASa6f1RPt7un_1AhRYe6TAsTgBD-hEr9m1ZfLuc1eFkg130_head
{
this:
np:hasAssertion
dgn-np:NP64073.RASa6f1RPt7un_1AhRYe6TAsTgBD-hEr9m1ZfLuc1eFkg130_assertion
;
np:hasProvenance
dgn-np:NP64073.RASa6f1RPt7un_1AhRYe6TAsTgBD-hEr9m1ZfLuc1eFkg130_provenance
;
np:hasPublicationInfo
dgn-np:NP64073.RASa6f1RPt7un_1AhRYe6TAsTgBD-hEr9m1ZfLuc1eFkg130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP64073.RASa6f1RPt7un_1AhRYe6TAsTgBD-hEr9m1ZfLuc1eFkg130_assertion
a
np:Assertion
.
dgn-np:NP64073.RASa6f1RPt7un_1AhRYe6TAsTgBD-hEr9m1ZfLuc1eFkg130_provenance
a
np:Provenance
.
dgn-np:NP64073.RASa6f1RPt7un_1AhRYe6TAsTgBD-hEr9m1ZfLuc1eFkg130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP64073.RASa6f1RPt7un_1AhRYe6TAsTgBD-hEr9m1ZfLuc1eFkg130_assertion
{
miriam-gene:1268
a
ncit:C16612
.
lld:C0028754
a
ncit:C7057
.
dgn-gda:DGN22b4e674e40e2bdef07dfce8f413bb80
sio:SIO_000628
miriam-gene:1268
,
lld:C0028754
;
a
sio:SIO_001122
.
}
dgn-np:NP64073.RASa6f1RPt7un_1AhRYe6TAsTgBD-hEr9m1ZfLuc1eFkg130_provenance
{
dgn-np:NP64073.RASa6f1RPt7un_1AhRYe6TAsTgBD-hEr9m1ZfLuc1eFkg130_assertion
dcterms:description
"[Genetic variants at CNR1 are associated with obesity-related phenotypes in men. The detection of polymorphic variants in genes involved in the process of fat accumulation may help identify specific targets for pharmacological treatment of obesity and related metabolic abnormalities.]. 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:17405839
;
prov:wasDerivedFrom
dgn-void:gad-20130706
;
prov:wasGeneratedBy
eco:ECO_0000203
.
dgn-void:gad-20130706
pav:importedOn
"2013-07-06"^^
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:NP64073.RASa6f1RPt7un_1AhRYe6TAsTgBD-hEr9m1ZfLuc1eFkg130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:32:30+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" .
}