@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP730095.RApjO7RIvfRUjR3tzn7y_4YCDt2wmW5H1LN1sNoHo4cVw
> .
@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:NP730095.RApjO7RIvfRUjR3tzn7y_4YCDt2wmW5H1LN1sNoHo4cVw130_head
{
this:
np:hasAssertion
dgn-np:NP730095.RApjO7RIvfRUjR3tzn7y_4YCDt2wmW5H1LN1sNoHo4cVw130_assertion
;
np:hasProvenance
dgn-np:NP730095.RApjO7RIvfRUjR3tzn7y_4YCDt2wmW5H1LN1sNoHo4cVw130_provenance
;
np:hasPublicationInfo
dgn-np:NP730095.RApjO7RIvfRUjR3tzn7y_4YCDt2wmW5H1LN1sNoHo4cVw130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP730095.RApjO7RIvfRUjR3tzn7y_4YCDt2wmW5H1LN1sNoHo4cVw130_assertion
a
np:Assertion
.
dgn-np:NP730095.RApjO7RIvfRUjR3tzn7y_4YCDt2wmW5H1LN1sNoHo4cVw130_provenance
a
np:Provenance
.
dgn-np:NP730095.RApjO7RIvfRUjR3tzn7y_4YCDt2wmW5H1LN1sNoHo4cVw130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP730095.RApjO7RIvfRUjR3tzn7y_4YCDt2wmW5H1LN1sNoHo4cVw130_assertion
{
miriam-gene:3630
a
ncit:C16612
.
lld:C0035078
a
ncit:C7057
.
dgn-gda:DGN3ec842acd3d7d1192fcd5d62153cb043
sio:SIO_000628
miriam-gene:3630
,
lld:C0035078
;
a
sio:SIO_001121
.
}
dgn-np:NP730095.RApjO7RIvfRUjR3tzn7y_4YCDt2wmW5H1LN1sNoHo4cVw130_provenance
{
dgn-np:NP730095.RApjO7RIvfRUjR3tzn7y_4YCDt2wmW5H1LN1sNoHo4cVw130_assertion
dcterms:description
"[Numerous crosses between hypertensive and normotensive strains have produced several quantitative trait loci (QTL) for blood pressure and other related phenotypes such as left ventricular hypertrophy, stroke, insulin resistance and kidney failure.]. 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:11095156
;
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:NP730095.RApjO7RIvfRUjR3tzn7y_4YCDt2wmW5H1LN1sNoHo4cVw130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:39:23+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" .
}