@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP488993.RAYSbRv2qGFUQYKiLDHmr3LYK-jlVobSBoSvgzmHzJt1s
> .
@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:NP488993.RAYSbRv2qGFUQYKiLDHmr3LYK-jlVobSBoSvgzmHzJt1s130_head
{
this:
np:hasAssertion
dgn-np:NP488993.RAYSbRv2qGFUQYKiLDHmr3LYK-jlVobSBoSvgzmHzJt1s130_assertion
;
np:hasProvenance
dgn-np:NP488993.RAYSbRv2qGFUQYKiLDHmr3LYK-jlVobSBoSvgzmHzJt1s130_provenance
;
np:hasPublicationInfo
dgn-np:NP488993.RAYSbRv2qGFUQYKiLDHmr3LYK-jlVobSBoSvgzmHzJt1s130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP488993.RAYSbRv2qGFUQYKiLDHmr3LYK-jlVobSBoSvgzmHzJt1s130_assertion
a
np:Assertion
.
dgn-np:NP488993.RAYSbRv2qGFUQYKiLDHmr3LYK-jlVobSBoSvgzmHzJt1s130_provenance
a
np:Provenance
.
dgn-np:NP488993.RAYSbRv2qGFUQYKiLDHmr3LYK-jlVobSBoSvgzmHzJt1s130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP488993.RAYSbRv2qGFUQYKiLDHmr3LYK-jlVobSBoSvgzmHzJt1s130_assertion
{
miriam-gene:79068
a
ncit:C16612
.
lld:C0311277
a
ncit:C7057
.
dgn-gda:DGNa884afd566ac070816bf6c6c1d85d975
sio:SIO_000628
miriam-gene:79068
,
lld:C0311277
;
a
sio:SIO_001121
.
}
dgn-np:NP488993.RAYSbRv2qGFUQYKiLDHmr3LYK-jlVobSBoSvgzmHzJt1s130_provenance
{
dgn-np:NP488993.RAYSbRv2qGFUQYKiLDHmr3LYK-jlVobSBoSvgzmHzJt1s130_assertion
dcterms:description
"[The C allele of the rs7204609 polymorphism in the FTO gene increased the chance for the presence of MetS, especially central obesity, and microalbuminuria, independently of energy and nutrient intakes in this sample of type 2 diabetic patients from Southern Brazil.]. 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:21741858
;
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:NP488993.RAYSbRv2qGFUQYKiLDHmr3LYK-jlVobSBoSvgzmHzJt1s130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:36:52+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" .
}