@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP282021.RAPvXEs_PlGnkjYJKVuuSrCssTl2VpQi5heIqqlGKTDFk
> .
@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:NP282021.RAPvXEs_PlGnkjYJKVuuSrCssTl2VpQi5heIqqlGKTDFk130_head
{
this:
np:hasAssertion
dgn-np:NP282021.RAPvXEs_PlGnkjYJKVuuSrCssTl2VpQi5heIqqlGKTDFk130_assertion
;
np:hasProvenance
dgn-np:NP282021.RAPvXEs_PlGnkjYJKVuuSrCssTl2VpQi5heIqqlGKTDFk130_provenance
;
np:hasPublicationInfo
dgn-np:NP282021.RAPvXEs_PlGnkjYJKVuuSrCssTl2VpQi5heIqqlGKTDFk130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP282021.RAPvXEs_PlGnkjYJKVuuSrCssTl2VpQi5heIqqlGKTDFk130_assertion
a
np:Assertion
.
dgn-np:NP282021.RAPvXEs_PlGnkjYJKVuuSrCssTl2VpQi5heIqqlGKTDFk130_provenance
a
np:Provenance
.
dgn-np:NP282021.RAPvXEs_PlGnkjYJKVuuSrCssTl2VpQi5heIqqlGKTDFk130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP282021.RAPvXEs_PlGnkjYJKVuuSrCssTl2VpQi5heIqqlGKTDFk130_assertion
{
miriam-gene:3630
a
ncit:C16612
.
lld:C0149721
a
ncit:C7057
.
dgn-gda:DGNe83dc36ab08906dd37f71dbd14dfa091
sio:SIO_000628
miriam-gene:3630
,
lld:C0149721
;
a
sio:SIO_001121
.
}
dgn-np:NP282021.RAPvXEs_PlGnkjYJKVuuSrCssTl2VpQi5heIqqlGKTDFk130_provenance
{
dgn-np:NP282021.RAPvXEs_PlGnkjYJKVuuSrCssTl2VpQi5heIqqlGKTDFk130_assertion
dcterms:description
"[Using numerous crosses between hypertensive and normotensive strains, investigators identified several quantitative trait loci (QTL) for blood pressure subphenotypes and for cardiovascular complications such as left ventricular hypertrophy, kidney failure, stroke, and insulin resistance.]. 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:10642293
;
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:NP282021.RAPvXEs_PlGnkjYJKVuuSrCssTl2VpQi5heIqqlGKTDFk130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:34:39+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" .
}