@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP888375.RAqCwhBL47vqbk1kDHIGued40ypNsEJB6ALzEF_AEm63E
> .
@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:NP888375.RAqCwhBL47vqbk1kDHIGued40ypNsEJB6ALzEF_AEm63E130_head
{
this:
np:hasAssertion
dgn-np:NP888375.RAqCwhBL47vqbk1kDHIGued40ypNsEJB6ALzEF_AEm63E130_assertion
;
np:hasProvenance
dgn-np:NP888375.RAqCwhBL47vqbk1kDHIGued40ypNsEJB6ALzEF_AEm63E130_provenance
;
np:hasPublicationInfo
dgn-np:NP888375.RAqCwhBL47vqbk1kDHIGued40ypNsEJB6ALzEF_AEm63E130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP888375.RAqCwhBL47vqbk1kDHIGued40ypNsEJB6ALzEF_AEm63E130_assertion
a
np:Assertion
.
dgn-np:NP888375.RAqCwhBL47vqbk1kDHIGued40ypNsEJB6ALzEF_AEm63E130_provenance
a
np:Provenance
.
dgn-np:NP888375.RAqCwhBL47vqbk1kDHIGued40ypNsEJB6ALzEF_AEm63E130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP888375.RAqCwhBL47vqbk1kDHIGued40ypNsEJB6ALzEF_AEm63E130_assertion
{
miriam-gene:4842
a
ncit:C16612
.
lld:C0149721
a
ncit:C7057
.
dgn-gda:DGNa9ed97bb167d07c50f2d61451eda27cd
sio:SIO_000628
miriam-gene:4842
,
lld:C0149721
;
a
sio:SIO_001121
.
}
dgn-np:NP888375.RAqCwhBL47vqbk1kDHIGued40ypNsEJB6ALzEF_AEm63E130_provenance
{
dgn-np:NP888375.RAqCwhBL47vqbk1kDHIGued40ypNsEJB6ALzEF_AEm63E130_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:NP888375.RAqCwhBL47vqbk1kDHIGued40ypNsEJB6ALzEF_AEm63E130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:41:06+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" .
}