@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP346592.RABsIh4PcXl4pI91s6hXQsGurpyLrPX_skqwDRpz1dbm0
> .
@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:NP346592.RABsIh4PcXl4pI91s6hXQsGurpyLrPX_skqwDRpz1dbm0130_head
{
this:
np:hasAssertion
dgn-np:NP346592.RABsIh4PcXl4pI91s6hXQsGurpyLrPX_skqwDRpz1dbm0130_assertion
;
np:hasProvenance
dgn-np:NP346592.RABsIh4PcXl4pI91s6hXQsGurpyLrPX_skqwDRpz1dbm0130_provenance
;
np:hasPublicationInfo
dgn-np:NP346592.RABsIh4PcXl4pI91s6hXQsGurpyLrPX_skqwDRpz1dbm0130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP346592.RABsIh4PcXl4pI91s6hXQsGurpyLrPX_skqwDRpz1dbm0130_assertion
a
np:Assertion
.
dgn-np:NP346592.RABsIh4PcXl4pI91s6hXQsGurpyLrPX_skqwDRpz1dbm0130_provenance
a
np:Provenance
.
dgn-np:NP346592.RABsIh4PcXl4pI91s6hXQsGurpyLrPX_skqwDRpz1dbm0130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP346592.RABsIh4PcXl4pI91s6hXQsGurpyLrPX_skqwDRpz1dbm0130_assertion
{
miriam-gene:100379198
a
ncit:C16612
.
lld:C0018799
a
ncit:C7057
.
dgn-gda:DGN9e1d9c1edbc3e1b6e1654dc7f0c47258
sio:SIO_000628
miriam-gene:100379198
,
lld:C0018799
;
a
sio:SIO_001121
.
}
dgn-np:NP346592.RABsIh4PcXl4pI91s6hXQsGurpyLrPX_skqwDRpz1dbm0130_provenance
{
dgn-np:NP346592.RABsIh4PcXl4pI91s6hXQsGurpyLrPX_skqwDRpz1dbm0130_assertion
dcterms:description
"[Development of a murine ECT would provide access to many existing models of cardiac disease and open the possibility of performing targeted genetic manipulation with the ability to directly assess contractile and molecular variables.]. 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:21566213
;
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:NP346592.RABsIh4PcXl4pI91s6hXQsGurpyLrPX_skqwDRpz1dbm0130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:35:23+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" .
}