@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP347053.RAz3Q8EL4Jfo7vL84uLMHtEwa2xSO43r57wawOImmqOEI
> .
@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:NP347053.RAz3Q8EL4Jfo7vL84uLMHtEwa2xSO43r57wawOImmqOEI130_head
{
this:
np:hasAssertion
dgn-np:NP347053.RAz3Q8EL4Jfo7vL84uLMHtEwa2xSO43r57wawOImmqOEI130_assertion
;
np:hasProvenance
dgn-np:NP347053.RAz3Q8EL4Jfo7vL84uLMHtEwa2xSO43r57wawOImmqOEI130_provenance
;
np:hasPublicationInfo
dgn-np:NP347053.RAz3Q8EL4Jfo7vL84uLMHtEwa2xSO43r57wawOImmqOEI130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP347053.RAz3Q8EL4Jfo7vL84uLMHtEwa2xSO43r57wawOImmqOEI130_assertion
a
np:Assertion
.
dgn-np:NP347053.RAz3Q8EL4Jfo7vL84uLMHtEwa2xSO43r57wawOImmqOEI130_provenance
a
np:Provenance
.
dgn-np:NP347053.RAz3Q8EL4Jfo7vL84uLMHtEwa2xSO43r57wawOImmqOEI130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP347053.RAz3Q8EL4Jfo7vL84uLMHtEwa2xSO43r57wawOImmqOEI130_assertion
{
miriam-gene:54551
a
ncit:C16612
.
lld:C0028754
a
ncit:C7057
.
dgn-gda:DGN9d77e12a7d528f1e74c2e7f4d3c8c3eb
sio:SIO_000628
miriam-gene:54551
,
lld:C0028754
;
a
sio:SIO_001121
.
}
dgn-np:NP347053.RAz3Q8EL4Jfo7vL84uLMHtEwa2xSO43r57wawOImmqOEI130_provenance
{
dgn-np:NP347053.RAz3Q8EL4Jfo7vL84uLMHtEwa2xSO43r57wawOImmqOEI130_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-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:NP347053.RAz3Q8EL4Jfo7vL84uLMHtEwa2xSO43r57wawOImmqOEI130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:35:24+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" .
}