@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP538785.RA0f0n3gbgZvcihWsNWnZLj93xgt_BD243zoBI54tZohM
> .
@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:NP538785.RA0f0n3gbgZvcihWsNWnZLj93xgt_BD243zoBI54tZohM130_head
{
this:
np:hasAssertion
dgn-np:NP538785.RA0f0n3gbgZvcihWsNWnZLj93xgt_BD243zoBI54tZohM130_assertion
;
np:hasProvenance
dgn-np:NP538785.RA0f0n3gbgZvcihWsNWnZLj93xgt_BD243zoBI54tZohM130_provenance
;
np:hasPublicationInfo
dgn-np:NP538785.RA0f0n3gbgZvcihWsNWnZLj93xgt_BD243zoBI54tZohM130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP538785.RA0f0n3gbgZvcihWsNWnZLj93xgt_BD243zoBI54tZohM130_assertion
a
np:Assertion
.
dgn-np:NP538785.RA0f0n3gbgZvcihWsNWnZLj93xgt_BD243zoBI54tZohM130_provenance
a
np:Provenance
.
dgn-np:NP538785.RA0f0n3gbgZvcihWsNWnZLj93xgt_BD243zoBI54tZohM130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP538785.RA0f0n3gbgZvcihWsNWnZLj93xgt_BD243zoBI54tZohM130_assertion
{
miriam-gene:54741
a
ncit:C16612
.
lld:C0006370
a
ncit:C7057
.
dgn-gda:DGN4169187386fbde1237bea8237ee7d8ea
sio:SIO_000628
miriam-gene:54741
,
lld:C0006370
;
a
sio:SIO_001121
.
}
dgn-np:NP538785.RA0f0n3gbgZvcihWsNWnZLj93xgt_BD243zoBI54tZohM130_provenance
{
dgn-np:NP538785.RA0f0n3gbgZvcihWsNWnZLj93xgt_BD243zoBI54tZohM130_assertion
dcterms:description
"[Melanocortin-4 receptor gene (MC4R) variants are associated with obesity and binge eating disorder (BED), whereas the more prevalent proopiomelanocortin (POMC) and leptin receptor gene (LEPR) mutations are rarely associated with obesity or BED.]. 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:15585384
;
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:NP538785.RA0f0n3gbgZvcihWsNWnZLj93xgt_BD243zoBI54tZohM130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:37:25+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" .
}