@prefix this: <
http://rdf.disgenet.org/resource/nanopub/NP1269321.RAC5Jrj20m610SNNlEB9RsixMcpc9hHmbMqi7QyE7IfIk
> .
@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/v4.0.0/void/
> .
dgn-np:NP1269321.RAC5Jrj20m610SNNlEB9RsixMcpc9hHmbMqi7QyE7IfIk130_head
{
this:
np:hasAssertion
dgn-np:NP1269321.RAC5Jrj20m610SNNlEB9RsixMcpc9hHmbMqi7QyE7IfIk130_assertion
;
np:hasProvenance
dgn-np:NP1269321.RAC5Jrj20m610SNNlEB9RsixMcpc9hHmbMqi7QyE7IfIk130_provenance
;
np:hasPublicationInfo
dgn-np:NP1269321.RAC5Jrj20m610SNNlEB9RsixMcpc9hHmbMqi7QyE7IfIk130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP1269321.RAC5Jrj20m610SNNlEB9RsixMcpc9hHmbMqi7QyE7IfIk130_assertion
a
np:Assertion
.
dgn-np:NP1269321.RAC5Jrj20m610SNNlEB9RsixMcpc9hHmbMqi7QyE7IfIk130_provenance
a
np:Provenance
.
dgn-np:NP1269321.RAC5Jrj20m610SNNlEB9RsixMcpc9hHmbMqi7QyE7IfIk130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP1269321.RAC5Jrj20m610SNNlEB9RsixMcpc9hHmbMqi7QyE7IfIk130_assertion
{
miriam-gene:79017
a
ncit:C16612
.
lld:C0020538
a
ncit:C7057
.
dgn-gda:DGN4f11fee4c452581cea66342c29412664
sio:SIO_000628
miriam-gene:79017
,
lld:C0020538
;
a
sio:SIO_001121
.
}
dgn-np:NP1269321.RAC5Jrj20m610SNNlEB9RsixMcpc9hHmbMqi7QyE7IfIk130_provenance
{
dgn-np:NP1269321.RAC5Jrj20m610SNNlEB9RsixMcpc9hHmbMqi7QyE7IfIk130_assertion
dcterms:description
"[Meanwhile, the haplotype TCC in the Han hypertensive patients and the haplotype GGC in the Mongolian patients had independent effects in increasing the risk for EH and maybe used as risk factors for predicting high blood pressure.]. 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:25748737
;
prov:wasDerivedFrom
dgn-void:befree-2016
;
prov:wasGeneratedBy
eco:ECO_0000203
.
dgn-void:befree-2016
pav:importedOn
"2016-02-19"^^
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:NP1269321.RAC5Jrj20m610SNNlEB9RsixMcpc9hHmbMqi7QyE7IfIk130_publicationInfo
{
this:
dcterms:created
"2016-05-13T12:51:21+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
"v4.0.0.0" .
dgn-void:disgenetv3.0rdf
pav:version
"v4.0.0" .
}