@prefix this: <
http://rdf.disgenet.org/resource/nanopub/NP59600.RAUTG-IR0MW5oo2MuGC_6d8-5hfrX5Gul_Om5ty4P4Uh0
> .
@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:NP59600.RAUTG-IR0MW5oo2MuGC_6d8-5hfrX5Gul_Om5ty4P4Uh0130_head
{
this:
np:hasAssertion
dgn-np:NP59600.RAUTG-IR0MW5oo2MuGC_6d8-5hfrX5Gul_Om5ty4P4Uh0130_assertion
;
np:hasProvenance
dgn-np:NP59600.RAUTG-IR0MW5oo2MuGC_6d8-5hfrX5Gul_Om5ty4P4Uh0130_provenance
;
np:hasPublicationInfo
dgn-np:NP59600.RAUTG-IR0MW5oo2MuGC_6d8-5hfrX5Gul_Om5ty4P4Uh0130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP59600.RAUTG-IR0MW5oo2MuGC_6d8-5hfrX5Gul_Om5ty4P4Uh0130_assertion
a
np:Assertion
.
dgn-np:NP59600.RAUTG-IR0MW5oo2MuGC_6d8-5hfrX5Gul_Om5ty4P4Uh0130_provenance
a
np:Provenance
.
dgn-np:NP59600.RAUTG-IR0MW5oo2MuGC_6d8-5hfrX5Gul_Om5ty4P4Uh0130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP59600.RAUTG-IR0MW5oo2MuGC_6d8-5hfrX5Gul_Om5ty4P4Uh0130_assertion
{
miriam-gene:185
a
ncit:C16612
.
lld:C0149721
a
ncit:C7057
.
dgn-gda:DGNaad86d74b8cb9c8c458f22200719886f
sio:SIO_000628
miriam-gene:185
,
lld:C0149721
;
a
sio:SIO_001122
.
}
dgn-np:NP59600.RAUTG-IR0MW5oo2MuGC_6d8-5hfrX5Gul_Om5ty4P4Uh0130_provenance
{
dgn-np:NP59600.RAUTG-IR0MW5oo2MuGC_6d8-5hfrX5Gul_Om5ty4P4Uh0130_assertion
dcterms:description
"[Severity of vasoregulatory endothelial dysfunction is associated with carriage of both 235T allele of ANG gene and 1166C allele of AT1R gene, in the latter case aggravated by significant adhesion of vascular endothelium.]. 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:19253715
;
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:NP59600.RAUTG-IR0MW5oo2MuGC_6d8-5hfrX5Gul_Om5ty4P4Uh0130_publicationInfo
{
this:
dcterms:created
"2015-08-25T14:38:12+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" .
}