@prefix this: <
http://rdf.disgenet.org/resource/nanopub/NP80012.RAVUBdLvJ_bZqNdl_29jQ_qu2TG_uvuHcsOeI7IYgrOhQ
> .
@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:NP80012.RAVUBdLvJ_bZqNdl_29jQ_qu2TG_uvuHcsOeI7IYgrOhQ130_head
{
this:
np:hasAssertion
dgn-np:NP80012.RAVUBdLvJ_bZqNdl_29jQ_qu2TG_uvuHcsOeI7IYgrOhQ130_assertion
;
np:hasProvenance
dgn-np:NP80012.RAVUBdLvJ_bZqNdl_29jQ_qu2TG_uvuHcsOeI7IYgrOhQ130_provenance
;
np:hasPublicationInfo
dgn-np:NP80012.RAVUBdLvJ_bZqNdl_29jQ_qu2TG_uvuHcsOeI7IYgrOhQ130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP80012.RAVUBdLvJ_bZqNdl_29jQ_qu2TG_uvuHcsOeI7IYgrOhQ130_assertion
a
np:Assertion
.
dgn-np:NP80012.RAVUBdLvJ_bZqNdl_29jQ_qu2TG_uvuHcsOeI7IYgrOhQ130_provenance
a
np:Provenance
.
dgn-np:NP80012.RAVUBdLvJ_bZqNdl_29jQ_qu2TG_uvuHcsOeI7IYgrOhQ130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP80012.RAVUBdLvJ_bZqNdl_29jQ_qu2TG_uvuHcsOeI7IYgrOhQ130_assertion
{
miriam-gene:4846
a
ncit:C16612
.
lld:C3178801
a
ncit:C7057
.
dgn-gda:DGNba5e243a0b75425899bc9436d02789dd
sio:SIO_000628
miriam-gene:4846
,
lld:C3178801
;
a
sio:SIO_001122
.
}
dgn-np:NP80012.RAVUBdLvJ_bZqNdl_29jQ_qu2TG_uvuHcsOeI7IYgrOhQ130_provenance
{
dgn-np:NP80012.RAVUBdLvJ_bZqNdl_29jQ_qu2TG_uvuHcsOeI7IYgrOhQ130_assertion
dcterms:description
"[ The intron 4ab insertion/deletion genotype was associated with isolated lacunar infarction. Haplotype and functional studies suggested that the protective effect of the 4a variant could be mediated through changes in eNOS promoter activity and increased ]. 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:14963277
;
prov:wasDerivedFrom
dgn-void:gad-20150221
;
prov:wasGeneratedBy
eco:ECO_0000203
.
dgn-void:gad-20150221
pav:importedOn
"2015-02-21"^^
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:NP80012.RAVUBdLvJ_bZqNdl_29jQ_qu2TG_uvuHcsOeI7IYgrOhQ130_publicationInfo
{
this:
dcterms:created
"2015-08-25T14:38:23+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" .
}