@prefix this: <
http://rdf.disgenet.org/resource/nanopub/NP220761.RAuwGXHfrIa2dR_h7-aHys_gP8H0ivB_v8a4UJwhnCjJk
> .
@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/v3.0.0/void/
> .
dgn-np:NP220761.RAuwGXHfrIa2dR_h7-aHys_gP8H0ivB_v8a4UJwhnCjJk130_head
{
this:
np:hasAssertion
dgn-np:NP220761.RAuwGXHfrIa2dR_h7-aHys_gP8H0ivB_v8a4UJwhnCjJk130_assertion
;
np:hasProvenance
dgn-np:NP220761.RAuwGXHfrIa2dR_h7-aHys_gP8H0ivB_v8a4UJwhnCjJk130_provenance
;
np:hasPublicationInfo
dgn-np:NP220761.RAuwGXHfrIa2dR_h7-aHys_gP8H0ivB_v8a4UJwhnCjJk130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP220761.RAuwGXHfrIa2dR_h7-aHys_gP8H0ivB_v8a4UJwhnCjJk130_assertion
a
np:Assertion
.
dgn-np:NP220761.RAuwGXHfrIa2dR_h7-aHys_gP8H0ivB_v8a4UJwhnCjJk130_provenance
a
np:Provenance
.
dgn-np:NP220761.RAuwGXHfrIa2dR_h7-aHys_gP8H0ivB_v8a4UJwhnCjJk130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP220761.RAuwGXHfrIa2dR_h7-aHys_gP8H0ivB_v8a4UJwhnCjJk130_assertion
{
miriam-gene:49
a
ncit:C16612
.
lld:C0003873
a
ncit:C7057
.
dgn-gda:DGN2c4dcc617cb3c55141621bb157ec24fc
sio:SIO_000628
miriam-gene:49
,
lld:C0003873
;
a
sio:SIO_001122
.
}
dgn-np:NP220761.RAuwGXHfrIa2dR_h7-aHys_gP8H0ivB_v8a4UJwhnCjJk130_provenance
{
dgn-np:NP220761.RAuwGXHfrIa2dR_h7-aHys_gP8H0ivB_v8a4UJwhnCjJk130_assertion
dcterms:description
"[1302 patients fulfilling the 1987 ACR classification criteria for RA were genotyped for the MHCIITA rs3087456 and rs4774 gene polymorphisms to determine the influence of MHCIITA variants in the development of CV events.]. 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:22272574
;
prov:wasDerivedFrom
dgn-void:befree-20150227
;
prov:wasGeneratedBy
eco:ECO_0000203
.
dgn-void:befree-20150227
pav:importedOn
"2015-02-27"^^
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:NP220761.RAuwGXHfrIa2dR_h7-aHys_gP8H0ivB_v8a4UJwhnCjJk130_publicationInfo
{
this:
dcterms:created
"2015-08-25T14:39:45+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
"v3.0.0.0" .
dgn-void:disgenetv3.0rdf
pav:version
"v3.0.0" .
}