@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP86249.RAzYojq7pdFjmnvpvzCIuIAihIWrBFF46stqA-fgNcOJM
> .
@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:NP86249.RAzYojq7pdFjmnvpvzCIuIAihIWrBFF46stqA-fgNcOJM130_head
{
this:
np:hasAssertion
dgn-np:NP86249.RAzYojq7pdFjmnvpvzCIuIAihIWrBFF46stqA-fgNcOJM130_assertion
;
np:hasProvenance
dgn-np:NP86249.RAzYojq7pdFjmnvpvzCIuIAihIWrBFF46stqA-fgNcOJM130_provenance
;
np:hasPublicationInfo
dgn-np:NP86249.RAzYojq7pdFjmnvpvzCIuIAihIWrBFF46stqA-fgNcOJM130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP86249.RAzYojq7pdFjmnvpvzCIuIAihIWrBFF46stqA-fgNcOJM130_assertion
a
np:Assertion
.
dgn-np:NP86249.RAzYojq7pdFjmnvpvzCIuIAihIWrBFF46stqA-fgNcOJM130_provenance
a
np:Provenance
.
dgn-np:NP86249.RAzYojq7pdFjmnvpvzCIuIAihIWrBFF46stqA-fgNcOJM130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP86249.RAzYojq7pdFjmnvpvzCIuIAihIWrBFF46stqA-fgNcOJM130_assertion
{
miriam-gene:3600
a
ncit:C16612
.
lld:C0028754
a
ncit:C7057
.
dgn-gda:DGN072de581d6d4816040b9ac3af3f974eb
sio:SIO_000628
miriam-gene:3600
,
lld:C0028754
;
a
sio:SIO_001122
.
}
dgn-np:NP86249.RAzYojq7pdFjmnvpvzCIuIAihIWrBFF46stqA-fgNcOJM130_provenance
{
dgn-np:NP86249.RAzYojq7pdFjmnvpvzCIuIAihIWrBFF46stqA-fgNcOJM130_assertion
dcterms:description
"[Our results suggest that large CNVs, especially rare deletions, confer risk of obesity in patients with moderate obesity and that genes impacted by large CNVs represent intriguing candidates for obesity that warrant further study.]. 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:20622171
;
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:NP86249.RAzYojq7pdFjmnvpvzCIuIAihIWrBFF46stqA-fgNcOJM130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:32:42+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" .
}