@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP126223.RAyWg5XjHACXKUljdpwjj7d_eatPOjUgP4DOxf6h2xFpc
> .
@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:NP126223.RAyWg5XjHACXKUljdpwjj7d_eatPOjUgP4DOxf6h2xFpc130_head
{
this:
np:hasAssertion
dgn-np:NP126223.RAyWg5XjHACXKUljdpwjj7d_eatPOjUgP4DOxf6h2xFpc130_assertion
;
np:hasProvenance
dgn-np:NP126223.RAyWg5XjHACXKUljdpwjj7d_eatPOjUgP4DOxf6h2xFpc130_provenance
;
np:hasPublicationInfo
dgn-np:NP126223.RAyWg5XjHACXKUljdpwjj7d_eatPOjUgP4DOxf6h2xFpc130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP126223.RAyWg5XjHACXKUljdpwjj7d_eatPOjUgP4DOxf6h2xFpc130_assertion
a
np:Assertion
.
dgn-np:NP126223.RAyWg5XjHACXKUljdpwjj7d_eatPOjUgP4DOxf6h2xFpc130_provenance
a
np:Provenance
.
dgn-np:NP126223.RAyWg5XjHACXKUljdpwjj7d_eatPOjUgP4DOxf6h2xFpc130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP126223.RAyWg5XjHACXKUljdpwjj7d_eatPOjUgP4DOxf6h2xFpc130_assertion
{
miriam-gene:4000
a
ncit:C16612
.
lld:C0007193
a
ncit:C7057
.
dgn-gda:DGNa916fb033aee1c8f58d4a702a606bdc7
sio:SIO_000628
miriam-gene:4000
,
lld:C0007193
;
a
sio:SIO_001122
.
}
dgn-np:NP126223.RAyWg5XjHACXKUljdpwjj7d_eatPOjUgP4DOxf6h2xFpc130_provenance
{
dgn-np:NP126223.RAyWg5XjHACXKUljdpwjj7d_eatPOjUgP4DOxf6h2xFpc130_assertion
dcterms:description
"[Review/occurring mutations in LMNA have been shown to be responsible for distinct diseases called laminopathies, including dilated cardiomyopathy with or without conduction defect and with or without variable skeletal muscle involvement.]. 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:15080529
;
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:NP126223.RAyWg5XjHACXKUljdpwjj7d_eatPOjUgP4DOxf6h2xFpc130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:33:05+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" .
}