@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP882192.RAuYns4qXWtEDK1Ex9cxhSQMyaMboqksq0qCe1nnUsH78
> .
@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:NP882192.RAuYns4qXWtEDK1Ex9cxhSQMyaMboqksq0qCe1nnUsH78130_head
{
this:
np:hasAssertion
dgn-np:NP882192.RAuYns4qXWtEDK1Ex9cxhSQMyaMboqksq0qCe1nnUsH78130_assertion
;
np:hasProvenance
dgn-np:NP882192.RAuYns4qXWtEDK1Ex9cxhSQMyaMboqksq0qCe1nnUsH78130_provenance
;
np:hasPublicationInfo
dgn-np:NP882192.RAuYns4qXWtEDK1Ex9cxhSQMyaMboqksq0qCe1nnUsH78130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP882192.RAuYns4qXWtEDK1Ex9cxhSQMyaMboqksq0qCe1nnUsH78130_assertion
a
np:Assertion
.
dgn-np:NP882192.RAuYns4qXWtEDK1Ex9cxhSQMyaMboqksq0qCe1nnUsH78130_provenance
a
np:Provenance
.
dgn-np:NP882192.RAuYns4qXWtEDK1Ex9cxhSQMyaMboqksq0qCe1nnUsH78130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP882192.RAuYns4qXWtEDK1Ex9cxhSQMyaMboqksq0qCe1nnUsH78130_assertion
{
miriam-gene:37
a
ncit:C16612
.
lld:C0018802
a
ncit:C7057
.
dgn-gda:DGN7e9e8ef32d7f9d280bad38ada439a779
sio:SIO_000628
miriam-gene:37
,
lld:C0018802
;
a
sio:SIO_001121
.
}
dgn-np:NP882192.RAuYns4qXWtEDK1Ex9cxhSQMyaMboqksq0qCe1nnUsH78130_provenance
{
dgn-np:NP882192.RAuYns4qXWtEDK1Ex9cxhSQMyaMboqksq0qCe1nnUsH78130_assertion
dcterms:description
"[Although VLCAD is relatively rare, timely and correct diagnosis leads to dramatic recovery, so that detection by newborn screening could prevent the onset of arrhythmias, heart failure, metabolic insufficiency, and death.]. 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:11433098
;
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:NP882192.RAuYns4qXWtEDK1Ex9cxhSQMyaMboqksq0qCe1nnUsH78130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:40:59+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" .
}