@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP523223.RAFJlEusD72oFY5tRfg8DbCmWmMBOZedijJBEEMu29_6E
> .
@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:NP523223.RAFJlEusD72oFY5tRfg8DbCmWmMBOZedijJBEEMu29_6E130_head
{
this:
np:hasAssertion
dgn-np:NP523223.RAFJlEusD72oFY5tRfg8DbCmWmMBOZedijJBEEMu29_6E130_assertion
;
np:hasProvenance
dgn-np:NP523223.RAFJlEusD72oFY5tRfg8DbCmWmMBOZedijJBEEMu29_6E130_provenance
;
np:hasPublicationInfo
dgn-np:NP523223.RAFJlEusD72oFY5tRfg8DbCmWmMBOZedijJBEEMu29_6E130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP523223.RAFJlEusD72oFY5tRfg8DbCmWmMBOZedijJBEEMu29_6E130_assertion
a
np:Assertion
.
dgn-np:NP523223.RAFJlEusD72oFY5tRfg8DbCmWmMBOZedijJBEEMu29_6E130_provenance
a
np:Provenance
.
dgn-np:NP523223.RAFJlEusD72oFY5tRfg8DbCmWmMBOZedijJBEEMu29_6E130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP523223.RAFJlEusD72oFY5tRfg8DbCmWmMBOZedijJBEEMu29_6E130_assertion
{
miriam-gene:7043
a
ncit:C16612
.
lld:C0349788
a
ncit:C7057
.
dgn-gda:DGN072fd44428548651f57034a407c18f7d
sio:SIO_000628
miriam-gene:7043
,
lld:C0349788
;
a
sio:SIO_001121
.
}
dgn-np:NP523223.RAFJlEusD72oFY5tRfg8DbCmWmMBOZedijJBEEMu29_6E130_provenance
{
dgn-np:NP523223.RAFJlEusD72oFY5tRfg8DbCmWmMBOZedijJBEEMu29_6E130_assertion
dcterms:description
"[Direct sequencing of DNA from individuals belonging to established ARVD1 families failed to detect causative mutations in exonic sequences of four genes (POMT2, TGFbeta3, KIAAA1036 and KIAA0759) expressed in the heart and which defects could possibly induce plasma membrane instability or apoptosis, key features of ARVD pathogenesis.]. 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:12529708
;
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:NP523223.RAFJlEusD72oFY5tRfg8DbCmWmMBOZedijJBEEMu29_6E130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:37:11+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" .
}