@prefix this: <
http://rdf.disgenet.org/resource/nanopub/NP1046239.RAnQv4n1Fu6-fE6KdqQeTBjkSdy_xg4_Ufv5bxVyhFPUQ
> .
@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/
> .
@prefix wi: <
http://purl.org/ontology/wi/core#
> .
@prefix prov: <
http://www.w3.org/ns/prov#
> .
@prefix pav: <
http://purl.org/pav/
> .
@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/resource/nanopub/
> .
@prefix dgn-gda: <
http://rdf.disgenet.org/resource/gda/
> .
@prefix dgn-void: <
http://rdf.disgenet.org/v4.0.0/void/
> .
dgn-np:NP1046239.RAnQv4n1Fu6-fE6KdqQeTBjkSdy_xg4_Ufv5bxVyhFPUQ130_head
{
this:
np:hasAssertion
dgn-np:NP1046239.RAnQv4n1Fu6-fE6KdqQeTBjkSdy_xg4_Ufv5bxVyhFPUQ130_assertion
;
np:hasProvenance
dgn-np:NP1046239.RAnQv4n1Fu6-fE6KdqQeTBjkSdy_xg4_Ufv5bxVyhFPUQ130_provenance
;
np:hasPublicationInfo
dgn-np:NP1046239.RAnQv4n1Fu6-fE6KdqQeTBjkSdy_xg4_Ufv5bxVyhFPUQ130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP1046239.RAnQv4n1Fu6-fE6KdqQeTBjkSdy_xg4_Ufv5bxVyhFPUQ130_assertion
a
np:Assertion
.
dgn-np:NP1046239.RAnQv4n1Fu6-fE6KdqQeTBjkSdy_xg4_Ufv5bxVyhFPUQ130_provenance
a
np:Provenance
.
dgn-np:NP1046239.RAnQv4n1Fu6-fE6KdqQeTBjkSdy_xg4_Ufv5bxVyhFPUQ130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP1046239.RAnQv4n1Fu6-fE6KdqQeTBjkSdy_xg4_Ufv5bxVyhFPUQ130_assertion
{
miriam-gene:2688
a
ncit:C16612
.
lld:C0028754
a
ncit:C7057
.
dgn-gda:DGNf77c0c01ca61015ddfa635623db05f32
sio:SIO_000628
miriam-gene:2688
,
lld:C0028754
;
a
sio:SIO_001121
.
}
dgn-np:NP1046239.RAnQv4n1Fu6-fE6KdqQeTBjkSdy_xg4_Ufv5bxVyhFPUQ130_provenance
{
dgn-np:NP1046239.RAnQv4n1Fu6-fE6KdqQeTBjkSdy_xg4_Ufv5bxVyhFPUQ130_assertion
dcterms:description
"[This neural defect, together with increased fat mass, blunted circadian rhythm, and growth hormone response pathway defects that are also linked to loss of MAGEL2, could contribute to the hyperphagia and obesity that are hallmarks of this disorder.]. 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:23341784
;
prov:wasDerivedFrom
dgn-void:befree-2016
;
prov:wasGeneratedBy
eco:ECO_0000203
.
dgn-void:befree-2016
pav:importedOn
"2016-02-19"^^
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:NP1046239.RAnQv4n1Fu6-fE6KdqQeTBjkSdy_xg4_Ufv5bxVyhFPUQ130_publicationInfo
{
this:
dcterms:created
"2016-05-13T12:49:40+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:disgenetv3.0rdf
;
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
"v4.0.0.0" .
dgn-void:disgenetv3.0rdf
pav:version
"v4.0.0" .
}