@prefix dc: <
http://purl.org/dc/terms/
> .
@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP79588.RAbRLtKTy6AJT0bIT_T0kyxZZJCP5jOe_XyEiu8uCgNaA
> .
@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 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#
> .
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{
this:
np:hasAssertion
dgn-np:NP79588.RAbRLtKTy6AJT0bIT_T0kyxZZJCP5jOe_XyEiu8uCgNaA130_assertion
;
np:hasProvenance
dgn-np:NP79588.RAbRLtKTy6AJT0bIT_T0kyxZZJCP5jOe_XyEiu8uCgNaA130_provenance
;
np:hasPublicationInfo
dgn-np:NP79588.RAbRLtKTy6AJT0bIT_T0kyxZZJCP5jOe_XyEiu8uCgNaA130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP79588.RAbRLtKTy6AJT0bIT_T0kyxZZJCP5jOe_XyEiu8uCgNaA130_assertion
a
np:Assertion
.
dgn-np:NP79588.RAbRLtKTy6AJT0bIT_T0kyxZZJCP5jOe_XyEiu8uCgNaA130_provenance
a
np:Provenance
.
dgn-np:NP79588.RAbRLtKTy6AJT0bIT_T0kyxZZJCP5jOe_XyEiu8uCgNaA130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP79588.RAbRLtKTy6AJT0bIT_T0kyxZZJCP5jOe_XyEiu8uCgNaA130_assertion
{
miriam-gene:727
a
ncit:C16612
.
lld:C0035439
a
ncit:C7057
.
dgn-gda:DGN106ff1dcf1fbc874a1195ffe71e22d9b
sio:SIO_000628
miriam-gene:727
,
lld:C0035439
;
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.
}
dgn-np:NP79588.RAbRLtKTy6AJT0bIT_T0kyxZZJCP5jOe_XyEiu8uCgNaA130_provenance
{
dgn-np:NP79588.RAbRLtKTy6AJT0bIT_T0kyxZZJCP5jOe_XyEiu8uCgNaA130_assertion
dc:description
"[We observed no association with RHD for the five tagging single nucleotide polymorphisms (tSNP) in the C5 gene, the three tSNPs in the TNFAIP3 gene, or the two tSNPs in the TRAF1 gene.]. 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:19902201
;
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:NP79588.RAbRLtKTy6AJT0bIT_T0kyxZZJCP5jOe_XyEiu8uCgNaA130_publicationInfo
{
this:
dc:created
"2014-10-02T12:32:39+02:00"^^
xsd:dateTime
;
dc:rights
<
http://opendatacommons.org/licenses/odbl/1.0/
> ;
dc:rightsHolder
dgn-void:IBIGroup
;
dc: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
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dgn-void:disgenetrdf
pav:version
"v2.1.0" .
}