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http://rdf.disgenet.org/nanopublications.trig#NP580839.RAREWBB1bMXLdnWHHzcJdqsopMVTaWUTxEkzuKVWNy_vs
> .
@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#
> .
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{
this:
np:hasAssertion
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;
np:hasProvenance
dgn-np:NP580839.RAREWBB1bMXLdnWHHzcJdqsopMVTaWUTxEkzuKVWNy_vs130_provenance
;
np:hasPublicationInfo
dgn-np:NP580839.RAREWBB1bMXLdnWHHzcJdqsopMVTaWUTxEkzuKVWNy_vs130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP580839.RAREWBB1bMXLdnWHHzcJdqsopMVTaWUTxEkzuKVWNy_vs130_assertion
a
np:Assertion
.
dgn-np:NP580839.RAREWBB1bMXLdnWHHzcJdqsopMVTaWUTxEkzuKVWNy_vs130_provenance
a
np:Provenance
.
dgn-np:NP580839.RAREWBB1bMXLdnWHHzcJdqsopMVTaWUTxEkzuKVWNy_vs130_publicationInfo
a
np:PublicationInfo
.
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dgn-np:NP580839.RAREWBB1bMXLdnWHHzcJdqsopMVTaWUTxEkzuKVWNy_vs130_assertion
{
miriam-gene:1825
a
ncit:C16612
.
lld:C0349788
a
ncit:C7057
.
dgn-gda:DGNa32c331a7c12ffb10b7e913f5fa11355
sio:SIO_000628
miriam-gene:1825
,
lld:C0349788
;
a
sio:SIO_001121
.
}
dgn-np:NP580839.RAREWBB1bMXLdnWHHzcJdqsopMVTaWUTxEkzuKVWNy_vs130_provenance
{
dgn-np:NP580839.RAREWBB1bMXLdnWHHzcJdqsopMVTaWUTxEkzuKVWNy_vs130_assertion
dcterms:description
"[We genotyped a cohort of 22 ARVC patients referred to molecular genetic screening in our heart center for mutations in the desmosomal candidate genes JUP, DSG2, DSC2, DSP and PKP2 known to be associated with ARVC.]. 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:20829228
;
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 .
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dgn-np:NP580839.RAREWBB1bMXLdnWHHzcJdqsopMVTaWUTxEkzuKVWNy_vs130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:37:50+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
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pav:authoredBy
<
http://orcid.org/0000-0001-5999-6269
> , <
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> , <
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" .
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"v2.1.0" .
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