@prefix this: <
http://rdf.disgenet.org/resource/nanopub/NP1383663.RA9drOhviNN9UfE--mdTmbRvspIdMdWlihILxdfxT3OhE
> .
@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:NP1383663.RA9drOhviNN9UfE--mdTmbRvspIdMdWlihILxdfxT3OhE130_head
{
this:
np:hasAssertion
dgn-np:NP1383663.RA9drOhviNN9UfE--mdTmbRvspIdMdWlihILxdfxT3OhE130_assertion
;
np:hasProvenance
dgn-np:NP1383663.RA9drOhviNN9UfE--mdTmbRvspIdMdWlihILxdfxT3OhE130_provenance
;
np:hasPublicationInfo
dgn-np:NP1383663.RA9drOhviNN9UfE--mdTmbRvspIdMdWlihILxdfxT3OhE130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP1383663.RA9drOhviNN9UfE--mdTmbRvspIdMdWlihILxdfxT3OhE130_assertion
a
np:Assertion
.
dgn-np:NP1383663.RA9drOhviNN9UfE--mdTmbRvspIdMdWlihILxdfxT3OhE130_provenance
a
np:Provenance
.
dgn-np:NP1383663.RA9drOhviNN9UfE--mdTmbRvspIdMdWlihILxdfxT3OhE130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP1383663.RA9drOhviNN9UfE--mdTmbRvspIdMdWlihILxdfxT3OhE130_assertion
{
miriam-gene:1636
a
ncit:C16612
.
lld:C0149721
a
ncit:C7057
.
dgn-gda:DGN933bbda97fca678eac804967dde73dd4
sio:SIO_000628
miriam-gene:1636
,
lld:C0149721
;
a
sio:SIO_001121
.
}
dgn-np:NP1383663.RA9drOhviNN9UfE--mdTmbRvspIdMdWlihILxdfxT3OhE130_provenance
{
dgn-np:NP1383663.RA9drOhviNN9UfE--mdTmbRvspIdMdWlihILxdfxT3OhE130_assertion
dcterms:description
"[In contrast to some previous studies, we have found in this group of previously untreated hypertensive subjects no evidence to suggest that the deletion polymorphism of the ACE genotype is important in the development of LVH.]. 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:9364280
;
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:NP1383663.RA9drOhviNN9UfE--mdTmbRvspIdMdWlihILxdfxT3OhE130_publicationInfo
{
this:
dcterms:created
"2016-05-13T12:52:13+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" .
}