@prefix this: <
http://rdf.disgenet.org/resource/nanopub/NP1269323.RApWm1KqDIfNYlhgWG9NMxt-SxITDdHALR5_2bckXD8Cw
> .
@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:NP1269323.RApWm1KqDIfNYlhgWG9NMxt-SxITDdHALR5_2bckXD8Cw130_head
{
this:
np:hasAssertion
dgn-np:NP1269323.RApWm1KqDIfNYlhgWG9NMxt-SxITDdHALR5_2bckXD8Cw130_assertion
;
np:hasProvenance
dgn-np:NP1269323.RApWm1KqDIfNYlhgWG9NMxt-SxITDdHALR5_2bckXD8Cw130_provenance
;
np:hasPublicationInfo
dgn-np:NP1269323.RApWm1KqDIfNYlhgWG9NMxt-SxITDdHALR5_2bckXD8Cw130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP1269323.RApWm1KqDIfNYlhgWG9NMxt-SxITDdHALR5_2bckXD8Cw130_assertion
a
np:Assertion
.
dgn-np:NP1269323.RApWm1KqDIfNYlhgWG9NMxt-SxITDdHALR5_2bckXD8Cw130_provenance
a
np:Provenance
.
dgn-np:NP1269323.RApWm1KqDIfNYlhgWG9NMxt-SxITDdHALR5_2bckXD8Cw130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP1269323.RApWm1KqDIfNYlhgWG9NMxt-SxITDdHALR5_2bckXD8Cw130_assertion
{
miriam-gene:79017
a
ncit:C16612
.
lld:C0085580
a
ncit:C7057
.
dgn-gda:DGN69058fdbf18808fb8f41104ca3622b52
sio:SIO_000628
miriam-gene:79017
,
lld:C0085580
;
a
sio:SIO_001121
.
}
dgn-np:NP1269323.RApWm1KqDIfNYlhgWG9NMxt-SxITDdHALR5_2bckXD8Cw130_provenance
{
dgn-np:NP1269323.RApWm1KqDIfNYlhgWG9NMxt-SxITDdHALR5_2bckXD8Cw130_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:NP1269323.RApWm1KqDIfNYlhgWG9NMxt-SxITDdHALR5_2bckXD8Cw130_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" .
}