@prefix dc: <
http://purl.org/dc/terms/
> .
@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP126224.RApjIPnheqYjzzFnXTLSoRqIlDV1n-9-btVNyj7rpzXIY
> .
@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 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:NP126224.RApjIPnheqYjzzFnXTLSoRqIlDV1n-9-btVNyj7rpzXIY130_head
{
this:
np:hasAssertion
dgn-np:NP126224.RApjIPnheqYjzzFnXTLSoRqIlDV1n-9-btVNyj7rpzXIY130_assertion
;
np:hasProvenance
dgn-np:NP126224.RApjIPnheqYjzzFnXTLSoRqIlDV1n-9-btVNyj7rpzXIY130_provenance
;
np:hasPublicationInfo
dgn-np:NP126224.RApjIPnheqYjzzFnXTLSoRqIlDV1n-9-btVNyj7rpzXIY130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP126224.RApjIPnheqYjzzFnXTLSoRqIlDV1n-9-btVNyj7rpzXIY130_assertion
a
np:Assertion
.
dgn-np:NP126224.RApjIPnheqYjzzFnXTLSoRqIlDV1n-9-btVNyj7rpzXIY130_provenance
a
np:Provenance
.
dgn-np:NP126224.RApjIPnheqYjzzFnXTLSoRqIlDV1n-9-btVNyj7rpzXIY130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP126224.RApjIPnheqYjzzFnXTLSoRqIlDV1n-9-btVNyj7rpzXIY130_assertion
{
miriam-gene:4000
a
ncit:C16612
.
lld:C0007193
a
ncit:C7057
.
dgn-gda:DGN8158f220abbbe658b688d5e29683b8a9
sio:SIO_000628
miriam-gene:4000
,
lld:C0007193
;
a
sio:SIO_001122
.
}
dgn-np:NP126224.RApjIPnheqYjzzFnXTLSoRqIlDV1n-9-btVNyj7rpzXIY130_provenance
{
dgn-np:NP126224.RApjIPnheqYjzzFnXTLSoRqIlDV1n-9-btVNyj7rpzXIY130_assertion
dc:description
"[D192G mutation in LMNA gene may lead to the disruption of the nuclear wall in cardiomyocytes, thus supporting the mechanical hypothesis of dilated cardiomyopathy development in humans, which might be mutation-specific.]. 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:18502446
;
prov:wasDerivedFrom
dgn-void:lhgdn-20090331
;
prov:wasGeneratedBy
eco:ECO_0000203
.
dgn-void:lhgdn-20090331
pav:importedOn
"2009-03-31"^^
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:NP126224.RApjIPnheqYjzzFnXTLSoRqIlDV1n-9-btVNyj7rpzXIY130_publicationInfo
{
this:
dc:created
"2014-10-02T12:33:05+02:00"^^
xsd:dateTime
;
dc:rights
<
http://opendatacommons.org/licenses/odbl/1.0/
> ;
dc:rightsHolder
dgn-void:IBIGroup
;
dc: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" .
}