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http://rdf.disgenet.org/nanopublications.trig#NP511900.RAyT8GEV1vZHS3gelQ5vZypBEc4ej5uqyRAY6LnkChyvY
> .
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http://www.w3.org/2000/01/rdf-schema#
> .
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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#
> .
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http://rdf.disgenet.org/v2.1.0/void.ttl#
> .
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{
this:
np:hasAssertion
dgn-np:NP511900.RAyT8GEV1vZHS3gelQ5vZypBEc4ej5uqyRAY6LnkChyvY130_assertion
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np:hasProvenance
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np:hasPublicationInfo
dgn-np:NP511900.RAyT8GEV1vZHS3gelQ5vZypBEc4ej5uqyRAY6LnkChyvY130_publicationInfo
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a
np:Nanopublication
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dgn-np:NP511900.RAyT8GEV1vZHS3gelQ5vZypBEc4ej5uqyRAY6LnkChyvY130_assertion
a
np:Assertion
.
dgn-np:NP511900.RAyT8GEV1vZHS3gelQ5vZypBEc4ej5uqyRAY6LnkChyvY130_provenance
a
np:Provenance
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dgn-np:NP511900.RAyT8GEV1vZHS3gelQ5vZypBEc4ej5uqyRAY6LnkChyvY130_publicationInfo
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dgn-np:NP511900.RAyT8GEV1vZHS3gelQ5vZypBEc4ej5uqyRAY6LnkChyvY130_assertion
{
miriam-gene:23026
a
ncit:C16612
.
lld:C0011847
a
ncit:C7057
.
dgn-gda:DGN30ee0d65ac8a8418c520b91dfec60ac5
sio:SIO_000628
miriam-gene:23026
,
lld:C0011847
;
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.
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dgn-np:NP511900.RAyT8GEV1vZHS3gelQ5vZypBEc4ej5uqyRAY6LnkChyvY130_provenance
{
dgn-np:NP511900.RAyT8GEV1vZHS3gelQ5vZypBEc4ej5uqyRAY6LnkChyvY130_assertion
dcterms:description
"[Thus, associations identified in the GoKinD collections on chromosomes 11p15.4 (near the CARS gene) and 13q33.3 (within an intergenic region between MYO16 and IRS2) are susceptibility loci of kidney disease common to both type 1 and 2 diabetes.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine."@en ;
wi:evidence
dgn-void:source_evidence_literature
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sio:SIO_000772
miriam-pubmed:21412220
;
prov:wasDerivedFrom
dgn-void:befree-20140225
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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 .
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dgn-np:NP511900.RAyT8GEV1vZHS3gelQ5vZypBEc4ej5uqyRAY6LnkChyvY130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:37:05+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
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<
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> , <
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> , <
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> ;
pav:createdBy
<
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pav:version
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