@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP250315.RA58Zgp4bMIboKbDdYo-ff779FitvMdwuZBAAbJnYGzZ0
> .
@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:NP250315.RA58Zgp4bMIboKbDdYo-ff779FitvMdwuZBAAbJnYGzZ0130_head
{
this:
np:hasAssertion
dgn-np:NP250315.RA58Zgp4bMIboKbDdYo-ff779FitvMdwuZBAAbJnYGzZ0130_assertion
;
np:hasProvenance
dgn-np:NP250315.RA58Zgp4bMIboKbDdYo-ff779FitvMdwuZBAAbJnYGzZ0130_provenance
;
np:hasPublicationInfo
dgn-np:NP250315.RA58Zgp4bMIboKbDdYo-ff779FitvMdwuZBAAbJnYGzZ0130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP250315.RA58Zgp4bMIboKbDdYo-ff779FitvMdwuZBAAbJnYGzZ0130_assertion
a
np:Assertion
.
dgn-np:NP250315.RA58Zgp4bMIboKbDdYo-ff779FitvMdwuZBAAbJnYGzZ0130_provenance
a
np:Provenance
.
dgn-np:NP250315.RA58Zgp4bMIboKbDdYo-ff779FitvMdwuZBAAbJnYGzZ0130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP250315.RA58Zgp4bMIboKbDdYo-ff779FitvMdwuZBAAbJnYGzZ0130_assertion
{
miriam-gene:4843
a
ncit:C16612
.
lld:C0038454
a
ncit:C7057
.
dgn-gda:DGN27ae343adecc69d5a876689c5050d7e6
sio:SIO_000628
miriam-gene:4843
,
lld:C0038454
;
a
sio:SIO_001121
.
}
dgn-np:NP250315.RA58Zgp4bMIboKbDdYo-ff779FitvMdwuZBAAbJnYGzZ0130_provenance
{
dgn-np:NP250315.RA58Zgp4bMIboKbDdYo-ff779FitvMdwuZBAAbJnYGzZ0130_assertion
dcterms:description
"[Because of lower endomyocardial NOS gene expression in patients with higher functional class and lower LV stroke work, increased endomyocardial NOS gene expression seems to be beneficial rather than detrimental for the failing heart.]. 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:11309529
;
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:NP250315.RA58Zgp4bMIboKbDdYo-ff779FitvMdwuZBAAbJnYGzZ0130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:34:20+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" .
}