@prefix this: <
http://rdf.disgenet.org/resource/nanopub/NP631787.RA2ZCQf7uje5F4AxuF3EM_VHeK6_R7cXV1EiVejaLCf0g
> .
@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/
> .
@prefix wi: <
http://purl.org/ontology/wi/core#
> .
@prefix prov: <
http://www.w3.org/ns/prov#
> .
@prefix pav: <
http://purl.org/pav/
> .
@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/resource/nanopub/
> .
@prefix dgn-gda: <
http://rdf.disgenet.org/resource/gda/
> .
@prefix dgn-void: <
http://rdf.disgenet.org/v4.0.0/void/
> .
dgn-np:NP631787.RA2ZCQf7uje5F4AxuF3EM_VHeK6_R7cXV1EiVejaLCf0g130_head
{
this:
np:hasAssertion
dgn-np:NP631787.RA2ZCQf7uje5F4AxuF3EM_VHeK6_R7cXV1EiVejaLCf0g130_assertion
;
np:hasProvenance
dgn-np:NP631787.RA2ZCQf7uje5F4AxuF3EM_VHeK6_R7cXV1EiVejaLCf0g130_provenance
;
np:hasPublicationInfo
dgn-np:NP631787.RA2ZCQf7uje5F4AxuF3EM_VHeK6_R7cXV1EiVejaLCf0g130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP631787.RA2ZCQf7uje5F4AxuF3EM_VHeK6_R7cXV1EiVejaLCf0g130_assertion
a
np:Assertion
.
dgn-np:NP631787.RA2ZCQf7uje5F4AxuF3EM_VHeK6_R7cXV1EiVejaLCf0g130_provenance
a
np:Provenance
.
dgn-np:NP631787.RA2ZCQf7uje5F4AxuF3EM_VHeK6_R7cXV1EiVejaLCf0g130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP631787.RA2ZCQf7uje5F4AxuF3EM_VHeK6_R7cXV1EiVejaLCf0g130_assertion
{
miriam-gene:3767
a
ncit:C16612
.
lld:C0011847
a
ncit:C7057
.
dgn-gda:DGN6c701b7889ff02fb830c57fabf5a82f9
sio:SIO_000628
miriam-gene:3767
,
lld:C0011847
;
a
sio:SIO_001121
.
}
dgn-np:NP631787.RA2ZCQf7uje5F4AxuF3EM_VHeK6_R7cXV1EiVejaLCf0g130_provenance
{
dgn-np:NP631787.RA2ZCQf7uje5F4AxuF3EM_VHeK6_R7cXV1EiVejaLCf0g130_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-2016
;
prov:wasGeneratedBy
eco:ECO_0000203
.
dgn-void:befree-2016
pav:importedOn
"2016-02-19"^^
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:NP631787.RA2ZCQf7uje5F4AxuF3EM_VHeK6_R7cXV1EiVejaLCf0g130_publicationInfo
{
this:
dcterms:created
"2016-05-13T12:46:32+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:disgenetv3.0rdf
;
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
"v4.0.0.0" .
dgn-void:disgenetv3.0rdf
pav:version
"v4.0.0" .
}