@prefix dct: <
http://purl.org/dc/terms/
> .
@prefix orcid: <
http://orcid.org/
> .
@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP58924.RAysJryeW2y_MCnw3IKTgNIn4ONrVYj_x8I6aZnUqDaHo
> .
@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:NP58924.RAysJryeW2y_MCnw3IKTgNIn4ONrVYj_x8I6aZnUqDaHo130_head
{
this:
np:hasAssertion
dgn-np:NP58924.RAysJryeW2y_MCnw3IKTgNIn4ONrVYj_x8I6aZnUqDaHo130_assertion
;
np:hasProvenance
dgn-np:NP58924.RAysJryeW2y_MCnw3IKTgNIn4ONrVYj_x8I6aZnUqDaHo130_provenance
;
np:hasPublicationInfo
dgn-np:NP58924.RAysJryeW2y_MCnw3IKTgNIn4ONrVYj_x8I6aZnUqDaHo130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP58924.RAysJryeW2y_MCnw3IKTgNIn4ONrVYj_x8I6aZnUqDaHo130_assertion
a
np:Assertion
.
dgn-np:NP58924.RAysJryeW2y_MCnw3IKTgNIn4ONrVYj_x8I6aZnUqDaHo130_provenance
a
np:Provenance
.
dgn-np:NP58924.RAysJryeW2y_MCnw3IKTgNIn4ONrVYj_x8I6aZnUqDaHo130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP58924.RAysJryeW2y_MCnw3IKTgNIn4ONrVYj_x8I6aZnUqDaHo130_assertion
{
miriam-gene:7350
a
ncit:C16612
.
lld:C0028754
a
ncit:C7057
.
dgn-gda:DGNb997e6c00b162b36f9dd17dd1a18bdb2
sio:SIO_000628
miriam-gene:7350
,
lld:C0028754
;
a
sio:SIO_001122
.
}
dgn-np:NP58924.RAysJryeW2y_MCnw3IKTgNIn4ONrVYj_x8I6aZnUqDaHo130_provenance
{
dgn-np:NP58924.RAysJryeW2y_MCnw3IKTgNIn4ONrVYj_x8I6aZnUqDaHo130_assertion
dct: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:NP58924.RAysJryeW2y_MCnw3IKTgNIn4ONrVYj_x8I6aZnUqDaHo130_publicationInfo
{
this:
dct:created
"2014-10-02T12:32:27+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" .
}