@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP348499.RAmezssfpo39z09PLf6Ib0lYukg7N1ivatTz2iP21OT8E
> .
@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:NP348499.RAmezssfpo39z09PLf6Ib0lYukg7N1ivatTz2iP21OT8E130_head
{
this:
np:hasAssertion
dgn-np:NP348499.RAmezssfpo39z09PLf6Ib0lYukg7N1ivatTz2iP21OT8E130_assertion
;
np:hasProvenance
dgn-np:NP348499.RAmezssfpo39z09PLf6Ib0lYukg7N1ivatTz2iP21OT8E130_provenance
;
np:hasPublicationInfo
dgn-np:NP348499.RAmezssfpo39z09PLf6Ib0lYukg7N1ivatTz2iP21OT8E130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP348499.RAmezssfpo39z09PLf6Ib0lYukg7N1ivatTz2iP21OT8E130_assertion
a
np:Assertion
.
dgn-np:NP348499.RAmezssfpo39z09PLf6Ib0lYukg7N1ivatTz2iP21OT8E130_provenance
a
np:Provenance
.
dgn-np:NP348499.RAmezssfpo39z09PLf6Ib0lYukg7N1ivatTz2iP21OT8E130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP348499.RAmezssfpo39z09PLf6Ib0lYukg7N1ivatTz2iP21OT8E130_assertion
{
miriam-gene:1825
a
ncit:C16612
.
lld:C0349788
a
ncit:C7057
.
dgn-gda:DGN6caccad4da4944a2d3632b3da2335928
sio:SIO_000628
miriam-gene:1825
,
lld:C0349788
;
a
sio:SIO_001121
.
}
dgn-np:NP348499.RAmezssfpo39z09PLf6Ib0lYukg7N1ivatTz2iP21OT8E130_provenance
{
dgn-np:NP348499.RAmezssfpo39z09PLf6Ib0lYukg7N1ivatTz2iP21OT8E130_assertion
dcterms:description
"[DNA sequencing revealed that each individual was heterozygous for two rare variants in the PKP2 and DSC2 genes, both of which were previously shown to be associated with ARVD and to encode desmosomal proteins, i.e.]. 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:21822014
;
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:NP348499.RAmezssfpo39z09PLf6Ib0lYukg7N1ivatTz2iP21OT8E130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:35:24+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" .
}