@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP372783.RAL0MV_qdVNl1JVw7lMxf7aDDYCCDwi622wYCqkQ6varc
> .
@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:NP372783.RAL0MV_qdVNl1JVw7lMxf7aDDYCCDwi622wYCqkQ6varc130_head
{
this:
np:hasAssertion
dgn-np:NP372783.RAL0MV_qdVNl1JVw7lMxf7aDDYCCDwi622wYCqkQ6varc130_assertion
;
np:hasProvenance
dgn-np:NP372783.RAL0MV_qdVNl1JVw7lMxf7aDDYCCDwi622wYCqkQ6varc130_provenance
;
np:hasPublicationInfo
dgn-np:NP372783.RAL0MV_qdVNl1JVw7lMxf7aDDYCCDwi622wYCqkQ6varc130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP372783.RAL0MV_qdVNl1JVw7lMxf7aDDYCCDwi622wYCqkQ6varc130_assertion
a
np:Assertion
.
dgn-np:NP372783.RAL0MV_qdVNl1JVw7lMxf7aDDYCCDwi622wYCqkQ6varc130_provenance
a
np:Provenance
.
dgn-np:NP372783.RAL0MV_qdVNl1JVw7lMxf7aDDYCCDwi622wYCqkQ6varc130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP372783.RAL0MV_qdVNl1JVw7lMxf7aDDYCCDwi622wYCqkQ6varc130_assertion
{
miriam-gene:4000
a
ncit:C16612
.
lld:C0018802
a
ncit:C7057
.
dgn-gda:DGNcc64fc3dd047cea6d2d0a7ea51fb585c
sio:SIO_000628
miriam-gene:4000
,
lld:C0018802
;
a
sio:SIO_001121
.
}
dgn-np:NP372783.RAL0MV_qdVNl1JVw7lMxf7aDDYCCDwi622wYCqkQ6varc130_provenance
{
dgn-np:NP372783.RAL0MV_qdVNl1JVw7lMxf7aDDYCCDwi622wYCqkQ6varc130_assertion
dcterms:description
"[The cardiac disease of LMNA mutated patients is classically defined by conduction system and rhythm disturbances occurring early in the course of the disease, followed by dilated cardiomyopathy and heart failure.]. 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:17067107
;
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:NP372783.RAL0MV_qdVNl1JVw7lMxf7aDDYCCDwi622wYCqkQ6varc130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:35:38+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" .
}