@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP48308.RAnEbII08A0vNWQ9gEgJTLmWSSvxDA1vXVRXDuagJQva4
> .
@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:NP48308.RAnEbII08A0vNWQ9gEgJTLmWSSvxDA1vXVRXDuagJQva4130_head
{
this:
np:hasAssertion
dgn-np:NP48308.RAnEbII08A0vNWQ9gEgJTLmWSSvxDA1vXVRXDuagJQva4130_assertion
;
np:hasProvenance
dgn-np:NP48308.RAnEbII08A0vNWQ9gEgJTLmWSSvxDA1vXVRXDuagJQva4130_provenance
;
np:hasPublicationInfo
dgn-np:NP48308.RAnEbII08A0vNWQ9gEgJTLmWSSvxDA1vXVRXDuagJQva4130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP48308.RAnEbII08A0vNWQ9gEgJTLmWSSvxDA1vXVRXDuagJQva4130_assertion
a
np:Assertion
.
dgn-np:NP48308.RAnEbII08A0vNWQ9gEgJTLmWSSvxDA1vXVRXDuagJQva4130_provenance
a
np:Provenance
.
dgn-np:NP48308.RAnEbII08A0vNWQ9gEgJTLmWSSvxDA1vXVRXDuagJQva4130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP48308.RAnEbII08A0vNWQ9gEgJTLmWSSvxDA1vXVRXDuagJQva4130_assertion
{
miriam-gene:348
a
ncit:C16612
.
lld:C0018099
a
ncit:C7057
.
dgn-gda:DGN6823088aac1191b9ff2753efe756fee5
sio:SIO_000628
miriam-gene:348
,
lld:C0018099
;
a
sio:SIO_001122
.
}
dgn-np:NP48308.RAnEbII08A0vNWQ9gEgJTLmWSSvxDA1vXVRXDuagJQva4130_provenance
{
dgn-np:NP48308.RAnEbII08A0vNWQ9gEgJTLmWSSvxDA1vXVRXDuagJQva4130_assertion
dcterms:description
"[ These results show that the reduced renal excretion of uric acid in patients with gout is mediated by high levels of VLDL and by the high prevalence of the E2 allele of apolipoprotein E.]. 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:12626798
;
prov:wasDerivedFrom
dgn-void:gad-20130706
;
prov:wasGeneratedBy
eco:ECO_0000203
.
dgn-void:gad-20130706
pav:importedOn
"2013-07-06"^^
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:NP48308.RAnEbII08A0vNWQ9gEgJTLmWSSvxDA1vXVRXDuagJQva4130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:32:22+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" .
}