@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP160326.RAu6E3pLxwN4rGyL9AkcufNAIVeCYsPt8svvUZQg0oKtQ
> .
@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:NP160326.RAu6E3pLxwN4rGyL9AkcufNAIVeCYsPt8svvUZQg0oKtQ130_head
{
this:
np:hasAssertion
dgn-np:NP160326.RAu6E3pLxwN4rGyL9AkcufNAIVeCYsPt8svvUZQg0oKtQ130_assertion
;
np:hasProvenance
dgn-np:NP160326.RAu6E3pLxwN4rGyL9AkcufNAIVeCYsPt8svvUZQg0oKtQ130_provenance
;
np:hasPublicationInfo
dgn-np:NP160326.RAu6E3pLxwN4rGyL9AkcufNAIVeCYsPt8svvUZQg0oKtQ130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP160326.RAu6E3pLxwN4rGyL9AkcufNAIVeCYsPt8svvUZQg0oKtQ130_assertion
a
np:Assertion
.
dgn-np:NP160326.RAu6E3pLxwN4rGyL9AkcufNAIVeCYsPt8svvUZQg0oKtQ130_provenance
a
np:Provenance
.
dgn-np:NP160326.RAu6E3pLxwN4rGyL9AkcufNAIVeCYsPt8svvUZQg0oKtQ130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP160326.RAu6E3pLxwN4rGyL9AkcufNAIVeCYsPt8svvUZQg0oKtQ130_assertion
{
miriam-gene:23209
a
ncit:C16612
.
lld:C0018801
a
ncit:C7057
.
dgn-gda:DGNc3a73d5d6d315a8bb9f29d42cd5a97fb
sio:SIO_000628
miriam-gene:23209
,
lld:C0018801
;
a
sio:SIO_001121
.
}
dgn-np:NP160326.RAu6E3pLxwN4rGyL9AkcufNAIVeCYsPt8svvUZQg0oKtQ130_provenance
{
dgn-np:NP160326.RAu6E3pLxwN4rGyL9AkcufNAIVeCYsPt8svvUZQg0oKtQ130_assertion
dcterms:description
"[The clinical syndrome of heart failure is associated with both a resting vasoconstriction and reduced sensitivity to nitric oxide mediated vasodilatation, and this review will focus on the role of myosin light chain (MLC) phosphatase in the pathogenesis of the vascular abnormalities of heart 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:19120700
;
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:NP160326.RAu6E3pLxwN4rGyL9AkcufNAIVeCYsPt8svvUZQg0oKtQ130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:33:26+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" .
}