@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP517850.RAeL2XMfJMpPQzaxMUiZGKuTSzyktuXTEp7UGVtl4_Qkg
> .
@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:NP517850.RAeL2XMfJMpPQzaxMUiZGKuTSzyktuXTEp7UGVtl4_Qkg130_head
{
this:
np:hasAssertion
dgn-np:NP517850.RAeL2XMfJMpPQzaxMUiZGKuTSzyktuXTEp7UGVtl4_Qkg130_assertion
;
np:hasProvenance
dgn-np:NP517850.RAeL2XMfJMpPQzaxMUiZGKuTSzyktuXTEp7UGVtl4_Qkg130_provenance
;
np:hasPublicationInfo
dgn-np:NP517850.RAeL2XMfJMpPQzaxMUiZGKuTSzyktuXTEp7UGVtl4_Qkg130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP517850.RAeL2XMfJMpPQzaxMUiZGKuTSzyktuXTEp7UGVtl4_Qkg130_assertion
a
np:Assertion
.
dgn-np:NP517850.RAeL2XMfJMpPQzaxMUiZGKuTSzyktuXTEp7UGVtl4_Qkg130_provenance
a
np:Provenance
.
dgn-np:NP517850.RAeL2XMfJMpPQzaxMUiZGKuTSzyktuXTEp7UGVtl4_Qkg130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP517850.RAeL2XMfJMpPQzaxMUiZGKuTSzyktuXTEp7UGVtl4_Qkg130_assertion
{
miriam-gene:4160
a
ncit:C16612
.
lld:C0028756
a
ncit:C7057
.
dgn-gda:DGN566b50e594ed73a1d67f963bb9910f31
sio:SIO_000628
miriam-gene:4160
,
lld:C0028756
;
a
sio:SIO_001121
.
}
dgn-np:NP517850.RAeL2XMfJMpPQzaxMUiZGKuTSzyktuXTEp7UGVtl4_Qkg130_provenance
{
dgn-np:NP517850.RAeL2XMfJMpPQzaxMUiZGKuTSzyktuXTEp7UGVtl4_Qkg130_assertion
dcterms:description
"[Systematic screening of 431 obese children and adults for mutations in the coding sequence and the minimal core promoter of MC4R reveals that genetic variation in the transcriptionally essential region of the MC4R promoter is not a significant cause of severe obesity in humans.]. 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:14633862
;
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:NP517850.RAeL2XMfJMpPQzaxMUiZGKuTSzyktuXTEp7UGVtl4_Qkg130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:37:08+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" .
}