@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP573057.RA4VtWGC_I_rdlWOKpamloC7cCMA_jRPfaP5LWlCZMWK0
> .
@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:NP573057.RA4VtWGC_I_rdlWOKpamloC7cCMA_jRPfaP5LWlCZMWK0130_head
{
this:
np:hasAssertion
dgn-np:NP573057.RA4VtWGC_I_rdlWOKpamloC7cCMA_jRPfaP5LWlCZMWK0130_assertion
;
np:hasProvenance
dgn-np:NP573057.RA4VtWGC_I_rdlWOKpamloC7cCMA_jRPfaP5LWlCZMWK0130_provenance
;
np:hasPublicationInfo
dgn-np:NP573057.RA4VtWGC_I_rdlWOKpamloC7cCMA_jRPfaP5LWlCZMWK0130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP573057.RA4VtWGC_I_rdlWOKpamloC7cCMA_jRPfaP5LWlCZMWK0130_assertion
a
np:Assertion
.
dgn-np:NP573057.RA4VtWGC_I_rdlWOKpamloC7cCMA_jRPfaP5LWlCZMWK0130_provenance
a
np:Provenance
.
dgn-np:NP573057.RA4VtWGC_I_rdlWOKpamloC7cCMA_jRPfaP5LWlCZMWK0130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP573057.RA4VtWGC_I_rdlWOKpamloC7cCMA_jRPfaP5LWlCZMWK0130_assertion
{
miriam-gene:4843
a
ncit:C16612
.
lld:C0149721
a
ncit:C7057
.
dgn-gda:DGN3af29d0763d3cc0a13a21de1a51e36f3
sio:SIO_000628
miriam-gene:4843
,
lld:C0149721
;
a
sio:SIO_001121
.
}
dgn-np:NP573057.RA4VtWGC_I_rdlWOKpamloC7cCMA_jRPfaP5LWlCZMWK0130_provenance
{
dgn-np:NP573057.RA4VtWGC_I_rdlWOKpamloC7cCMA_jRPfaP5LWlCZMWK0130_assertion
dcterms:description
"[These results provide the first direct evidence that the complete disruption of all NOSs results in LV hypertrophy and diastolic dysfunction in mice in vivo through the AT(1) receptor pathway, demonstrating a pivotal role of the endogenous NOS system in maintaining cardiac homeostasis.]. 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:20966596
;
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:NP573057.RA4VtWGC_I_rdlWOKpamloC7cCMA_jRPfaP5LWlCZMWK0130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:37:45+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" .
}