@prefix this: <
http://rdf.disgenet.org/resource/nanopub/NP677130.RAhzpEuR8vmQsoW0oyFDo-vbD3NMqmej58Ql6BRjYRqMA
> .
@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/
> .
@prefix wi: <
http://purl.org/ontology/wi/core#
> .
@prefix prov: <
http://www.w3.org/ns/prov#
> .
@prefix pav: <
http://purl.org/pav/
> .
@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/resource/nanopub/
> .
@prefix dgn-gda: <
http://rdf.disgenet.org/resource/gda/
> .
@prefix dgn-void: <
http://rdf.disgenet.org/v3.0.0/void/
> .
dgn-np:NP677130.RAhzpEuR8vmQsoW0oyFDo-vbD3NMqmej58Ql6BRjYRqMA130_head
{
this:
np:hasAssertion
dgn-np:NP677130.RAhzpEuR8vmQsoW0oyFDo-vbD3NMqmej58Ql6BRjYRqMA130_assertion
;
np:hasProvenance
dgn-np:NP677130.RAhzpEuR8vmQsoW0oyFDo-vbD3NMqmej58Ql6BRjYRqMA130_provenance
;
np:hasPublicationInfo
dgn-np:NP677130.RAhzpEuR8vmQsoW0oyFDo-vbD3NMqmej58Ql6BRjYRqMA130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP677130.RAhzpEuR8vmQsoW0oyFDo-vbD3NMqmej58Ql6BRjYRqMA130_assertion
a
np:Assertion
.
dgn-np:NP677130.RAhzpEuR8vmQsoW0oyFDo-vbD3NMqmej58Ql6BRjYRqMA130_provenance
a
np:Provenance
.
dgn-np:NP677130.RAhzpEuR8vmQsoW0oyFDo-vbD3NMqmej58Ql6BRjYRqMA130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP677130.RAhzpEuR8vmQsoW0oyFDo-vbD3NMqmej58Ql6BRjYRqMA130_assertion
{
miriam-gene:6262
a
ncit:C16612
.
lld:C1631597
a
ncit:C7057
.
dgn-gda:DGNe1ca44736189e61e8701c4bacbe8d143
sio:SIO_000628
miriam-gene:6262
,
lld:C1631597
;
a
sio:SIO_001121
.
}
dgn-np:NP677130.RAhzpEuR8vmQsoW0oyFDo-vbD3NMqmej58Ql6BRjYRqMA130_provenance
{
dgn-np:NP677130.RAhzpEuR8vmQsoW0oyFDo-vbD3NMqmej58Ql6BRjYRqMA130_assertion
dcterms:description
"[One-hundred sixteen relatives carrying the Ryr2 mutation from 15 families who were identified by cascade screening of the Ryr2 mutation causing CPVT in the proband were clinically characterized, including 61 relatives from 1 family.]. 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:22787013
;
prov:wasDerivedFrom
dgn-void:befree-20150227
;
prov:wasGeneratedBy
eco:ECO_0000203
.
dgn-void:befree-20150227
pav:importedOn
"2015-02-27"^^
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:NP677130.RAhzpEuR8vmQsoW0oyFDo-vbD3NMqmej58Ql6BRjYRqMA130_publicationInfo
{
this:
dcterms:created
"2015-08-25T14:44:28+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:disgenetv3.0rdf
;
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
"v3.0.0.0" .
dgn-void:disgenetv3.0rdf
pav:version
"v3.0.0" .
}