@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP545063.RAOQucq_sxavybufE81a4diqaNdp-QrmzLd7K9GujoWz8
> .
@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#
> .
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{
this:
np:hasAssertion
dgn-np:NP545063.RAOQucq_sxavybufE81a4diqaNdp-QrmzLd7K9GujoWz8130_assertion
;
np:hasProvenance
dgn-np:NP545063.RAOQucq_sxavybufE81a4diqaNdp-QrmzLd7K9GujoWz8130_provenance
;
np:hasPublicationInfo
dgn-np:NP545063.RAOQucq_sxavybufE81a4diqaNdp-QrmzLd7K9GujoWz8130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP545063.RAOQucq_sxavybufE81a4diqaNdp-QrmzLd7K9GujoWz8130_assertion
a
np:Assertion
.
dgn-np:NP545063.RAOQucq_sxavybufE81a4diqaNdp-QrmzLd7K9GujoWz8130_provenance
a
np:Provenance
.
dgn-np:NP545063.RAOQucq_sxavybufE81a4diqaNdp-QrmzLd7K9GujoWz8130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP545063.RAOQucq_sxavybufE81a4diqaNdp-QrmzLd7K9GujoWz8130_assertion
{
miriam-gene:257194
a
ncit:C16612
.
lld:C0028754
a
ncit:C7057
.
dgn-gda:DGN18081a00dd1aa989749db5c08248effc
sio:SIO_000628
miriam-gene:257194
,
lld:C0028754
;
a
sio:SIO_001121
.
}
dgn-np:NP545063.RAOQucq_sxavybufE81a4diqaNdp-QrmzLd7K9GujoWz8130_provenance
{
dgn-np:NP545063.RAOQucq_sxavybufE81a4diqaNdp-QrmzLd7K9GujoWz8130_assertion
dcterms:description
"[Variants of TMEM18 and FTO are associated with obesity indices during puberty in Chinese children, but candidate SNPs of NEGR1, GNPDA2, MTCH2, SH2B1, MC4R and KCTD15 have no significant effects on obesity indices.]. 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:22083549
;
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:NP545063.RAOQucq_sxavybufE81a4diqaNdp-QrmzLd7K9GujoWz8130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:37:28+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" .
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"v2.1.0" .
}