@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP167790.RATn4ZDFPrJYjgiwEnj7prLhh6QzEANF4GvlJY78r26u4
> .
@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:NP167790.RATn4ZDFPrJYjgiwEnj7prLhh6QzEANF4GvlJY78r26u4130_head
{
this:
np:hasAssertion
dgn-np:NP167790.RATn4ZDFPrJYjgiwEnj7prLhh6QzEANF4GvlJY78r26u4130_assertion
;
np:hasProvenance
dgn-np:NP167790.RATn4ZDFPrJYjgiwEnj7prLhh6QzEANF4GvlJY78r26u4130_provenance
;
np:hasPublicationInfo
dgn-np:NP167790.RATn4ZDFPrJYjgiwEnj7prLhh6QzEANF4GvlJY78r26u4130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP167790.RATn4ZDFPrJYjgiwEnj7prLhh6QzEANF4GvlJY78r26u4130_assertion
a
np:Assertion
.
dgn-np:NP167790.RATn4ZDFPrJYjgiwEnj7prLhh6QzEANF4GvlJY78r26u4130_provenance
a
np:Provenance
.
dgn-np:NP167790.RATn4ZDFPrJYjgiwEnj7prLhh6QzEANF4GvlJY78r26u4130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP167790.RATn4ZDFPrJYjgiwEnj7prLhh6QzEANF4GvlJY78r26u4130_assertion
{
miriam-gene:5972
a
ncit:C16612
.
lld:C0020538
a
ncit:C7057
.
dgn-gda:DGN5785bd5fb3afc1d60ff5148a1a886cd6
sio:SIO_000628
miriam-gene:5972
,
lld:C0020538
;
a
sio:SIO_001121
.
}
dgn-np:NP167790.RATn4ZDFPrJYjgiwEnj7prLhh6QzEANF4GvlJY78r26u4130_provenance
{
dgn-np:NP167790.RATn4ZDFPrJYjgiwEnj7prLhh6QzEANF4GvlJY78r26u4130_assertion
dcterms:description
"[We developed a model of spontaneously high human renin hypertension in the rat by producing two transgenic strains, one for human angiotensinogen with the endogenous promoter and one for human renin with the endogenous promoter.]. 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:9039138
;
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:NP167790.RATn4ZDFPrJYjgiwEnj7prLhh6QzEANF4GvlJY78r26u4130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:33:30+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" .
}