@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP532973.RA_HQjIybhNKox-6Z0JzN_MxEThc-qwy6v0h4ZnBoWZv4
> .
@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:NP532973.RA_HQjIybhNKox-6Z0JzN_MxEThc-qwy6v0h4ZnBoWZv4130_head
{
this:
np:hasAssertion
dgn-np:NP532973.RA_HQjIybhNKox-6Z0JzN_MxEThc-qwy6v0h4ZnBoWZv4130_assertion
;
np:hasProvenance
dgn-np:NP532973.RA_HQjIybhNKox-6Z0JzN_MxEThc-qwy6v0h4ZnBoWZv4130_provenance
;
np:hasPublicationInfo
dgn-np:NP532973.RA_HQjIybhNKox-6Z0JzN_MxEThc-qwy6v0h4ZnBoWZv4130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP532973.RA_HQjIybhNKox-6Z0JzN_MxEThc-qwy6v0h4ZnBoWZv4130_assertion
a
np:Assertion
.
dgn-np:NP532973.RA_HQjIybhNKox-6Z0JzN_MxEThc-qwy6v0h4ZnBoWZv4130_provenance
a
np:Provenance
.
dgn-np:NP532973.RA_HQjIybhNKox-6Z0JzN_MxEThc-qwy6v0h4ZnBoWZv4130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP532973.RA_HQjIybhNKox-6Z0JzN_MxEThc-qwy6v0h4ZnBoWZv4130_assertion
{
miriam-gene:154
a
ncit:C16612
.
lld:C0149721
a
ncit:C7057
.
dgn-gda:DGN5c0e360fc33011f67b823dda243853b0
sio:SIO_000628
miriam-gene:154
,
lld:C0149721
;
a
sio:SIO_001121
.
}
dgn-np:NP532973.RA_HQjIybhNKox-6Z0JzN_MxEThc-qwy6v0h4ZnBoWZv4130_provenance
{
dgn-np:NP532973.RA_HQjIybhNKox-6Z0JzN_MxEThc-qwy6v0h4ZnBoWZv4130_assertion
dcterms:description
"[In a prospective follow-up study we screened 970 hypertensive patients of Caucasian descent for the Gly16Arg, Gln27Glu, and Thr164Ile beta(2)AR polymorphisms and left ventricular echocardiographic hypertrophy and assigned selected patients to enalapril or atenolol to assess left ventricular hypertrophy regression after 2-year follow-up.]. 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:17178264
;
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:NP532973.RA_HQjIybhNKox-6Z0JzN_MxEThc-qwy6v0h4ZnBoWZv4130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:37:22+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" .
}