@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP524594.RAdKOAc2uiR7FyJgJVFM6_Q9eZUeo21ZfML-nuBn2LlWE
> .
@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:NP524594.RAdKOAc2uiR7FyJgJVFM6_Q9eZUeo21ZfML-nuBn2LlWE130_head
{
this:
np:hasAssertion
dgn-np:NP524594.RAdKOAc2uiR7FyJgJVFM6_Q9eZUeo21ZfML-nuBn2LlWE130_assertion
;
np:hasProvenance
dgn-np:NP524594.RAdKOAc2uiR7FyJgJVFM6_Q9eZUeo21ZfML-nuBn2LlWE130_provenance
;
np:hasPublicationInfo
dgn-np:NP524594.RAdKOAc2uiR7FyJgJVFM6_Q9eZUeo21ZfML-nuBn2LlWE130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP524594.RAdKOAc2uiR7FyJgJVFM6_Q9eZUeo21ZfML-nuBn2LlWE130_assertion
a
np:Assertion
.
dgn-np:NP524594.RAdKOAc2uiR7FyJgJVFM6_Q9eZUeo21ZfML-nuBn2LlWE130_provenance
a
np:Provenance
.
dgn-np:NP524594.RAdKOAc2uiR7FyJgJVFM6_Q9eZUeo21ZfML-nuBn2LlWE130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP524594.RAdKOAc2uiR7FyJgJVFM6_Q9eZUeo21ZfML-nuBn2LlWE130_assertion
{
miriam-gene:1284
a
ncit:C16612
.
lld:C3272363
a
ncit:C7057
.
dgn-gda:DGN7a96d1777913734adfdda72c483639d4
sio:SIO_000628
miriam-gene:1284
,
lld:C3272363
;
a
sio:SIO_001121
.
}
dgn-np:NP524594.RAdKOAc2uiR7FyJgJVFM6_Q9eZUeo21ZfML-nuBn2LlWE130_provenance
{
dgn-np:NP524594.RAdKOAc2uiR7FyJgJVFM6_Q9eZUeo21ZfML-nuBn2LlWE130_assertion
dcterms:description
"[We investigated whether variants within a larger set of oxidative phosphorylation (OXPHOS) genes encoded by both autosomal and mitochondrial DNA were associated with risk of IS and, based on our results, extended our investigation to intracerebral hemorrhage (ICH).]. 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:23362085
;
prov:wasDerivedFrom
dgn-void:befree-20140225
;
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 .
}
dgn-np:NP524594.RAdKOAc2uiR7FyJgJVFM6_Q9eZUeo21ZfML-nuBn2LlWE130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:37:14+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" .
}