@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP271318.RArKfrNJugjN9M8cdLZEGgRomvj86xFL4oyP2NrpQVIcA
> .
@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:NP271318.RArKfrNJugjN9M8cdLZEGgRomvj86xFL4oyP2NrpQVIcA130_head
{
this:
np:hasAssertion
dgn-np:NP271318.RArKfrNJugjN9M8cdLZEGgRomvj86xFL4oyP2NrpQVIcA130_assertion
;
np:hasProvenance
dgn-np:NP271318.RArKfrNJugjN9M8cdLZEGgRomvj86xFL4oyP2NrpQVIcA130_provenance
;
np:hasPublicationInfo
dgn-np:NP271318.RArKfrNJugjN9M8cdLZEGgRomvj86xFL4oyP2NrpQVIcA130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP271318.RArKfrNJugjN9M8cdLZEGgRomvj86xFL4oyP2NrpQVIcA130_assertion
a
np:Assertion
.
dgn-np:NP271318.RArKfrNJugjN9M8cdLZEGgRomvj86xFL4oyP2NrpQVIcA130_provenance
a
np:Provenance
.
dgn-np:NP271318.RArKfrNJugjN9M8cdLZEGgRomvj86xFL4oyP2NrpQVIcA130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP271318.RArKfrNJugjN9M8cdLZEGgRomvj86xFL4oyP2NrpQVIcA130_assertion
{
miriam-gene:3172
a
ncit:C16612
.
lld:C0011847
a
ncit:C7057
.
dgn-gda:DGNe53f5cbf8c1cc2cda7054fe1e7d14ad3
sio:SIO_000628
miriam-gene:3172
,
lld:C0011847
;
a
sio:SIO_001121
.
}
dgn-np:NP271318.RArKfrNJugjN9M8cdLZEGgRomvj86xFL4oyP2NrpQVIcA130_provenance
{
dgn-np:NP271318.RArKfrNJugjN9M8cdLZEGgRomvj86xFL4oyP2NrpQVIcA130_assertion
dcterms:description
"[Carrying the minor alleles of the three HNF4A polymorphisms was associated with significantly greater diabetes risk in women carrying the KCNJ11 allele 23K, but not in those who did not carry this allele.]. 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:17894829
;
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:NP271318.RArKfrNJugjN9M8cdLZEGgRomvj86xFL4oyP2NrpQVIcA130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:34:31+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" .
}