@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP181809.RA62PZXZGwo3A7gQF5fGIaqTSr5I4DKs_-fAOhXrBSweU
> .
@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:NP181809.RA62PZXZGwo3A7gQF5fGIaqTSr5I4DKs_-fAOhXrBSweU130_head
{
this:
np:hasAssertion
dgn-np:NP181809.RA62PZXZGwo3A7gQF5fGIaqTSr5I4DKs_-fAOhXrBSweU130_assertion
;
np:hasProvenance
dgn-np:NP181809.RA62PZXZGwo3A7gQF5fGIaqTSr5I4DKs_-fAOhXrBSweU130_provenance
;
np:hasPublicationInfo
dgn-np:NP181809.RA62PZXZGwo3A7gQF5fGIaqTSr5I4DKs_-fAOhXrBSweU130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP181809.RA62PZXZGwo3A7gQF5fGIaqTSr5I4DKs_-fAOhXrBSweU130_assertion
a
np:Assertion
.
dgn-np:NP181809.RA62PZXZGwo3A7gQF5fGIaqTSr5I4DKs_-fAOhXrBSweU130_provenance
a
np:Provenance
.
dgn-np:NP181809.RA62PZXZGwo3A7gQF5fGIaqTSr5I4DKs_-fAOhXrBSweU130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP181809.RA62PZXZGwo3A7gQF5fGIaqTSr5I4DKs_-fAOhXrBSweU130_assertion
{
miriam-gene:3172
a
ncit:C16612
.
lld:C0011849
a
ncit:C7057
.
dgn-gda:DGN8f33625b0131ff6a366d4d5f6fb95450
sio:SIO_000628
miriam-gene:3172
,
lld:C0011849
;
a
sio:SIO_001121
.
}
dgn-np:NP181809.RA62PZXZGwo3A7gQF5fGIaqTSr5I4DKs_-fAOhXrBSweU130_provenance
{
dgn-np:NP181809.RA62PZXZGwo3A7gQF5fGIaqTSr5I4DKs_-fAOhXrBSweU130_assertion
dcterms:description
"[Nine SNPs spanning the HNF4 alpha P2 promoter (rs4810424, rs1884613 and rs1884614) and coding region (rs2144908, rs6031551, rs6031552, rs1885088, rs1028583 and rs3818247) were genotyped in 160 subjects without diabetes or metabolic syndrome.]. 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:21633728
;
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:NP181809.RA62PZXZGwo3A7gQF5fGIaqTSr5I4DKs_-fAOhXrBSweU130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:33:38+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" .
}