@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP79449.RAAYbxMHdOcyLjKqzoijtmXtpsOMXUJ2kG7Uc5XIpZ0kM
> .
@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:NP79449.RAAYbxMHdOcyLjKqzoijtmXtpsOMXUJ2kG7Uc5XIpZ0kM130_assertion
;
np:hasProvenance
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np:hasPublicationInfo
dgn-np:NP79449.RAAYbxMHdOcyLjKqzoijtmXtpsOMXUJ2kG7Uc5XIpZ0kM130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP79449.RAAYbxMHdOcyLjKqzoijtmXtpsOMXUJ2kG7Uc5XIpZ0kM130_assertion
a
np:Assertion
.
dgn-np:NP79449.RAAYbxMHdOcyLjKqzoijtmXtpsOMXUJ2kG7Uc5XIpZ0kM130_provenance
a
np:Provenance
.
dgn-np:NP79449.RAAYbxMHdOcyLjKqzoijtmXtpsOMXUJ2kG7Uc5XIpZ0kM130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP79449.RAAYbxMHdOcyLjKqzoijtmXtpsOMXUJ2kG7Uc5XIpZ0kM130_assertion
{
miriam-gene:776
a
ncit:C16612
.
lld:C0020538
a
ncit:C7057
.
dgn-gda:DGNbb383adce7aa48be3cf281ef51d6e8a0
sio:SIO_000628
miriam-gene:776
,
lld:C0020538
;
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sio:SIO_001122
.
}
dgn-np:NP79449.RAAYbxMHdOcyLjKqzoijtmXtpsOMXUJ2kG7Uc5XIpZ0kM130_provenance
{
dgn-np:NP79449.RAAYbxMHdOcyLjKqzoijtmXtpsOMXUJ2kG7Uc5XIpZ0kM130_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:gad-20130706
;
prov:wasGeneratedBy
eco:ECO_0000203
.
dgn-void:gad-20130706
pav:importedOn
"2013-07-06"^^
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:NP79449.RAAYbxMHdOcyLjKqzoijtmXtpsOMXUJ2kG7Uc5XIpZ0kM130_publicationInfo
{
this:
dcterms:created
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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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> , <
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> , <
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> , <
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> , <
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> ;
pav:createdBy
<
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> ;
pav:version
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dgn-void:disgenetrdf
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}