@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP653926.RAPUUcqpRdZ6P9QfvypNXxIE7n8eBPoz9DaCr2C7tI5So
> .
@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#
> .
dgn-np:NP653926.RAPUUcqpRdZ6P9QfvypNXxIE7n8eBPoz9DaCr2C7tI5So130_head
{
this:
np:hasAssertion
dgn-np:NP653926.RAPUUcqpRdZ6P9QfvypNXxIE7n8eBPoz9DaCr2C7tI5So130_assertion
;
np:hasProvenance
dgn-np:NP653926.RAPUUcqpRdZ6P9QfvypNXxIE7n8eBPoz9DaCr2C7tI5So130_provenance
;
np:hasPublicationInfo
dgn-np:NP653926.RAPUUcqpRdZ6P9QfvypNXxIE7n8eBPoz9DaCr2C7tI5So130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP653926.RAPUUcqpRdZ6P9QfvypNXxIE7n8eBPoz9DaCr2C7tI5So130_assertion
a
np:Assertion
.
dgn-np:NP653926.RAPUUcqpRdZ6P9QfvypNXxIE7n8eBPoz9DaCr2C7tI5So130_provenance
a
np:Provenance
.
dgn-np:NP653926.RAPUUcqpRdZ6P9QfvypNXxIE7n8eBPoz9DaCr2C7tI5So130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP653926.RAPUUcqpRdZ6P9QfvypNXxIE7n8eBPoz9DaCr2C7tI5So130_assertion
{
miriam-gene:775
a
ncit:C16612
.
lld:C0085580
a
ncit:C7057
.
dgn-gda:DGNa12293239010db849e3a61f6a2cfd09c
sio:SIO_000628
miriam-gene:775
,
lld:C0085580
;
a
sio:SIO_001121
.
}
dgn-np:NP653926.RAPUUcqpRdZ6P9QfvypNXxIE7n8eBPoz9DaCr2C7tI5So130_provenance
{
dgn-np:NP653926.RAPUUcqpRdZ6P9QfvypNXxIE7n8eBPoz9DaCr2C7tI5So130_assertion
dcterms:description
"[A pharmacogenomic analysis was undertaken in 161 patients with essential hypertension who were treated with dCCBs to study whether genetic polymorphisms of the calcium channel alpha1C and alpha1D subunit genes, CACNA1C and CACNA1D, are associated with the antihypertensive effects of dCCBs.]. 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:19225208
;
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:NP653926.RAPUUcqpRdZ6P9QfvypNXxIE7n8eBPoz9DaCr2C7tI5So130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:38:34+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
<
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
"v2.1.0.0" .
dgn-void:disgenetrdf
pav:version
"v2.1.0" .
}