@prefix dct: <
http://purl.org/dc/terms/
> .
@prefix orcid: <
http://orcid.org/
> .
@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP43445.RAuNn8G8Q8hP1cI9SYmrZF3i47e-jBCUZ_YyJE3j3qST0
> .
@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 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:NP43445.RAuNn8G8Q8hP1cI9SYmrZF3i47e-jBCUZ_YyJE3j3qST0130_head
{
this:
np:hasAssertion
dgn-np:NP43445.RAuNn8G8Q8hP1cI9SYmrZF3i47e-jBCUZ_YyJE3j3qST0130_assertion
;
np:hasProvenance
dgn-np:NP43445.RAuNn8G8Q8hP1cI9SYmrZF3i47e-jBCUZ_YyJE3j3qST0130_provenance
;
np:hasPublicationInfo
dgn-np:NP43445.RAuNn8G8Q8hP1cI9SYmrZF3i47e-jBCUZ_YyJE3j3qST0130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP43445.RAuNn8G8Q8hP1cI9SYmrZF3i47e-jBCUZ_YyJE3j3qST0130_assertion
a
np:Assertion
.
dgn-np:NP43445.RAuNn8G8Q8hP1cI9SYmrZF3i47e-jBCUZ_YyJE3j3qST0130_provenance
a
np:Provenance
.
dgn-np:NP43445.RAuNn8G8Q8hP1cI9SYmrZF3i47e-jBCUZ_YyJE3j3qST0130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP43445.RAuNn8G8Q8hP1cI9SYmrZF3i47e-jBCUZ_YyJE3j3qST0130_assertion
{
miriam-gene:2847
a
ncit:C16612
.
lld:C0028754
a
ncit:C7057
.
dgn-gda:DGNbd8a3878caef809f52c3dd5fe75c8b56
sio:SIO_000628
miriam-gene:2847
,
lld:C0028754
;
a
sio:SIO_001122
.
}
dgn-np:NP43445.RAuNn8G8Q8hP1cI9SYmrZF3i47e-jBCUZ_YyJE3j3qST0130_provenance
{
dgn-np:NP43445.RAuNn8G8Q8hP1cI9SYmrZF3i47e-jBCUZ_YyJE3j3qST0130_assertion
dct:description
"[In conclusion, mutations in the MCH receptors are not commonly found in humans with severe early onset obesity. Clarification of the relationship of these variants to obesity must await study in other populations and/or in genetically modified mice.]. 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:15166293
;
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:NP43445.RAuNn8G8Q8hP1cI9SYmrZF3i47e-jBCUZ_YyJE3j3qST0130_publicationInfo
{
this:
dct:created
"2014-10-02T12:32:19+02:00"^^
xsd:dateTime
;
dct:rights
<
http://opendatacommons.org/licenses/odbl/1.0/
> ;
dct:rightsHolder
dgn-void:IBIGroup
;
dct:subject
sio:SIO_000983
;
prv:usedData
dgn-void:disgenetrdf
;
pav:authoredBy
orcid:0000-0001-5999-6269
,
orcid:0000-0002-7534-7661
,
orcid:0000-0002-9383-528X
,
orcid:0000-0003-0169-8159
,
orcid:0000-0003-1244-7654
;
pav:createdBy
orcid:0000-0003-0169-8159
;
pav:version
"v2.1.0.0" .
dgn-void:disgenetrdf
pav:version
"v2.1.0" .
}