@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP255677.RAeHuDyMfRJPmDn4nCdiLDsbtjSbv99qJ0aNiJ_0oYd-c
> .
@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#
> .
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{
this:
np:hasAssertion
dgn-np:NP255677.RAeHuDyMfRJPmDn4nCdiLDsbtjSbv99qJ0aNiJ_0oYd-c130_assertion
;
np:hasProvenance
dgn-np:NP255677.RAeHuDyMfRJPmDn4nCdiLDsbtjSbv99qJ0aNiJ_0oYd-c130_provenance
;
np:hasPublicationInfo
dgn-np:NP255677.RAeHuDyMfRJPmDn4nCdiLDsbtjSbv99qJ0aNiJ_0oYd-c130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP255677.RAeHuDyMfRJPmDn4nCdiLDsbtjSbv99qJ0aNiJ_0oYd-c130_assertion
a
np:Assertion
.
dgn-np:NP255677.RAeHuDyMfRJPmDn4nCdiLDsbtjSbv99qJ0aNiJ_0oYd-c130_provenance
a
np:Provenance
.
dgn-np:NP255677.RAeHuDyMfRJPmDn4nCdiLDsbtjSbv99qJ0aNiJ_0oYd-c130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP255677.RAeHuDyMfRJPmDn4nCdiLDsbtjSbv99qJ0aNiJ_0oYd-c130_assertion
{
miriam-gene:6559
a
ncit:C16612
.
lld:C0020538
a
ncit:C7057
.
dgn-gda:DGNc1e322fdf470e2e649f81451b6c7ed35
sio:SIO_000628
miriam-gene:6559
,
lld:C0020538
;
a
sio:SIO_001121
.
}
dgn-np:NP255677.RAeHuDyMfRJPmDn4nCdiLDsbtjSbv99qJ0aNiJ_0oYd-c130_provenance
{
dgn-np:NP255677.RAeHuDyMfRJPmDn4nCdiLDsbtjSbv99qJ0aNiJ_0oYd-c130_assertion
dcterms:description
"[Here we tested whether STK39, OXSR1, and SLC12A3 genetically contribute to hypertension in the Han Chinese population and how the SNP to SNP or SNP to other risk factors interacts in the pathogenesis of hypertension.]. 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:20889219
;
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:NP255677.RAeHuDyMfRJPmDn4nCdiLDsbtjSbv99qJ0aNiJ_0oYd-c130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:34:23+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:disgenetrdf
;
pav:authoredBy
<
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> , <
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" .
}