@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP892097.RAsvStIf0RIi8pKpsugWdDZBOzbx4dj2dDmD3SLVC4ebQ
> .
@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:NP892097.RAsvStIf0RIi8pKpsugWdDZBOzbx4dj2dDmD3SLVC4ebQ130_head
{
this:
np:hasAssertion
dgn-np:NP892097.RAsvStIf0RIi8pKpsugWdDZBOzbx4dj2dDmD3SLVC4ebQ130_assertion
;
np:hasProvenance
dgn-np:NP892097.RAsvStIf0RIi8pKpsugWdDZBOzbx4dj2dDmD3SLVC4ebQ130_provenance
;
np:hasPublicationInfo
dgn-np:NP892097.RAsvStIf0RIi8pKpsugWdDZBOzbx4dj2dDmD3SLVC4ebQ130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP892097.RAsvStIf0RIi8pKpsugWdDZBOzbx4dj2dDmD3SLVC4ebQ130_assertion
a
np:Assertion
.
dgn-np:NP892097.RAsvStIf0RIi8pKpsugWdDZBOzbx4dj2dDmD3SLVC4ebQ130_provenance
a
np:Provenance
.
dgn-np:NP892097.RAsvStIf0RIi8pKpsugWdDZBOzbx4dj2dDmD3SLVC4ebQ130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP892097.RAsvStIf0RIi8pKpsugWdDZBOzbx4dj2dDmD3SLVC4ebQ130_assertion
{
miriam-gene:6520
a
ncit:C16612
.
lld:C0011860
a
ncit:C7057
.
dgn-gda:DGN4d352bfef4cbf6e0e813197a717f9f8b
sio:SIO_000628
miriam-gene:6520
,
lld:C0011860
;
a
sio:SIO_001121
.
}
dgn-np:NP892097.RAsvStIf0RIi8pKpsugWdDZBOzbx4dj2dDmD3SLVC4ebQ130_provenance
{
dgn-np:NP892097.RAsvStIf0RIi8pKpsugWdDZBOzbx4dj2dDmD3SLVC4ebQ130_assertion
dcterms:description
"[These gene differences were consistent with reported differences after stroke in areas such as injury and inflammation markers, the myosin heavy chain profile, and high prevalence of impaired glucose tolerance and type 2 diabetes.]. 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:18566945
;
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:NP892097.RAsvStIf0RIi8pKpsugWdDZBOzbx4dj2dDmD3SLVC4ebQ130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:41:08+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" .
}