@prefix bfo: <
http://purl.obolibrary.org/obo/
> .
@prefix this: <
http://rdf.disgenet.org/resource/nanopub/NP238127.RAPDg9-O-Hif9tM-FIs7kXzr2wxZm_JRw2drrl8sCoOuM
> .
@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 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:NP238127.RAPDg9-O-Hif9tM-FIs7kXzr2wxZm_JRw2drrl8sCoOuM130_head
{
this:
np:hasAssertion
dgn-np:NP238127.RAPDg9-O-Hif9tM-FIs7kXzr2wxZm_JRw2drrl8sCoOuM130_assertion
;
np:hasProvenance
dgn-np:NP238127.RAPDg9-O-Hif9tM-FIs7kXzr2wxZm_JRw2drrl8sCoOuM130_provenance
;
np:hasPublicationInfo
dgn-np:NP238127.RAPDg9-O-Hif9tM-FIs7kXzr2wxZm_JRw2drrl8sCoOuM130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP238127.RAPDg9-O-Hif9tM-FIs7kXzr2wxZm_JRw2drrl8sCoOuM130_assertion
a
np:Assertion
.
dgn-np:NP238127.RAPDg9-O-Hif9tM-FIs7kXzr2wxZm_JRw2drrl8sCoOuM130_provenance
a
np:Provenance
.
dgn-np:NP238127.RAPDg9-O-Hif9tM-FIs7kXzr2wxZm_JRw2drrl8sCoOuM130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP238127.RAPDg9-O-Hif9tM-FIs7kXzr2wxZm_JRw2drrl8sCoOuM130_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:NP238127.RAPDg9-O-Hif9tM-FIs7kXzr2wxZm_JRw2drrl8sCoOuM130_provenance
{
dgn-np:NP238127.RAPDg9-O-Hif9tM-FIs7kXzr2wxZm_JRw2drrl8sCoOuM130_assertion
dcterms: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
bfo:ECO_0000203
.
dgn-void:lhgdn-20090331
pav:importedOn
"2009-03-31"^^
xsd:date
.
dgn-void:source_evidence_literature
a
bfo:ECO_0000212
;
rdfs:comment
"Gene-disease associations inferred from text-mining the literature."@en ;
rdfs:label
"DisGeNET evidence - LITERATURE"@en .
}
dgn-np:NP238127.RAPDg9-O-Hif9tM-FIs7kXzr2wxZm_JRw2drrl8sCoOuM130_publicationInfo
{
this:
dcterms:created
"2016-05-13T12:43:34+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" .
}