@prefix this: <
http://rdf.disgenet.org/resource/nanopub/NP673076.RAjCT4JReUyCucT92X66i7mhK4YYqorzEob214QUiZsy0
> .
@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/
> .
@prefix wi: <
http://purl.org/ontology/wi/core#
> .
@prefix prov: <
http://www.w3.org/ns/prov#
> .
@prefix pav: <
http://purl.org/pav/
> .
@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/resource/nanopub/
> .
@prefix dgn-gda: <
http://rdf.disgenet.org/resource/gda/
> .
@prefix dgn-void: <
http://rdf.disgenet.org/v4.0.0/void/
> .
dgn-np:NP673076.RAjCT4JReUyCucT92X66i7mhK4YYqorzEob214QUiZsy0130_head
{
this:
np:hasAssertion
dgn-np:NP673076.RAjCT4JReUyCucT92X66i7mhK4YYqorzEob214QUiZsy0130_assertion
;
np:hasProvenance
dgn-np:NP673076.RAjCT4JReUyCucT92X66i7mhK4YYqorzEob214QUiZsy0130_provenance
;
np:hasPublicationInfo
dgn-np:NP673076.RAjCT4JReUyCucT92X66i7mhK4YYqorzEob214QUiZsy0130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP673076.RAjCT4JReUyCucT92X66i7mhK4YYqorzEob214QUiZsy0130_assertion
a
np:Assertion
.
dgn-np:NP673076.RAjCT4JReUyCucT92X66i7mhK4YYqorzEob214QUiZsy0130_provenance
a
np:Provenance
.
dgn-np:NP673076.RAjCT4JReUyCucT92X66i7mhK4YYqorzEob214QUiZsy0130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP673076.RAjCT4JReUyCucT92X66i7mhK4YYqorzEob214QUiZsy0130_assertion
{
miriam-gene:4000
a
ncit:C16612
.
lld:C0007193
a
ncit:C7057
.
dgn-gda:DGN2112173d0515f01a305d0e26740fba5f
sio:SIO_000628
miriam-gene:4000
,
lld:C0007193
;
a
sio:SIO_001122
.
}
dgn-np:NP673076.RAjCT4JReUyCucT92X66i7mhK4YYqorzEob214QUiZsy0130_provenance
{
dgn-np:NP673076.RAjCT4JReUyCucT92X66i7mhK4YYqorzEob214QUiZsy0130_assertion
dcterms:description
"[The study documents that 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:befree-2016
;
prov:wasGeneratedBy
eco:ECO_0000203
.
dgn-void:befree-2016
pav:importedOn
"2016-02-19"^^
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:NP673076.RAjCT4JReUyCucT92X66i7mhK4YYqorzEob214QUiZsy0130_publicationInfo
{
this:
dcterms:created
"2016-05-13T12:46:50+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:disgenetv3.0rdf
;
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
"v4.0.0.0" .
dgn-void:disgenetv3.0rdf
pav:version
"v4.0.0" .
}