@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP321065.RAacDfE9Xk7icu9EJ-3GK-Kd-wk9FzP_W_M-XCeq9Y_zo
> .
@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:NP321065.RAacDfE9Xk7icu9EJ-3GK-Kd-wk9FzP_W_M-XCeq9Y_zo130_head
{
this:
np:hasAssertion
dgn-np:NP321065.RAacDfE9Xk7icu9EJ-3GK-Kd-wk9FzP_W_M-XCeq9Y_zo130_assertion
;
np:hasProvenance
dgn-np:NP321065.RAacDfE9Xk7icu9EJ-3GK-Kd-wk9FzP_W_M-XCeq9Y_zo130_provenance
;
np:hasPublicationInfo
dgn-np:NP321065.RAacDfE9Xk7icu9EJ-3GK-Kd-wk9FzP_W_M-XCeq9Y_zo130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP321065.RAacDfE9Xk7icu9EJ-3GK-Kd-wk9FzP_W_M-XCeq9Y_zo130_assertion
a
np:Assertion
.
dgn-np:NP321065.RAacDfE9Xk7icu9EJ-3GK-Kd-wk9FzP_W_M-XCeq9Y_zo130_provenance
a
np:Provenance
.
dgn-np:NP321065.RAacDfE9Xk7icu9EJ-3GK-Kd-wk9FzP_W_M-XCeq9Y_zo130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP321065.RAacDfE9Xk7icu9EJ-3GK-Kd-wk9FzP_W_M-XCeq9Y_zo130_assertion
{
miriam-gene:4000
a
ncit:C16612
.
lld:C0004245
a
ncit:C7057
.
dgn-gda:DGNae7ca2f1da155e55c0f014616387bf5f
sio:SIO_000628
miriam-gene:4000
,
lld:C0004245
;
a
sio:SIO_001121
.
}
dgn-np:NP321065.RAacDfE9Xk7icu9EJ-3GK-Kd-wk9FzP_W_M-XCeq9Y_zo130_provenance
{
dgn-np:NP321065.RAacDfE9Xk7icu9EJ-3GK-Kd-wk9FzP_W_M-XCeq9Y_zo130_assertion
dcterms:description
"[Even though mutations in LMNA have been reported in patients with typical dilated cardiomyopathy (DCM) and atrioventricular block (AVB) previously, the purpose of this study was to disclose this novel genetic abnormality in one Chinese family with the atypical phenotype of progressive AVB followed by DCM with normal QRS interval.]. 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:20155465
;
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:NP321065.RAacDfE9Xk7icu9EJ-3GK-Kd-wk9FzP_W_M-XCeq9Y_zo130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:35:06+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" .
}