@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP657257.RA5QddsXGStMBA9yCONOqyv68RFNfeJ5GmJhHEG2WSlCY
> .
@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:NP657257.RA5QddsXGStMBA9yCONOqyv68RFNfeJ5GmJhHEG2WSlCY130_head
{
this:
np:hasAssertion
dgn-np:NP657257.RA5QddsXGStMBA9yCONOqyv68RFNfeJ5GmJhHEG2WSlCY130_assertion
;
np:hasProvenance
dgn-np:NP657257.RA5QddsXGStMBA9yCONOqyv68RFNfeJ5GmJhHEG2WSlCY130_provenance
;
np:hasPublicationInfo
dgn-np:NP657257.RA5QddsXGStMBA9yCONOqyv68RFNfeJ5GmJhHEG2WSlCY130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP657257.RA5QddsXGStMBA9yCONOqyv68RFNfeJ5GmJhHEG2WSlCY130_assertion
a
np:Assertion
.
dgn-np:NP657257.RA5QddsXGStMBA9yCONOqyv68RFNfeJ5GmJhHEG2WSlCY130_provenance
a
np:Provenance
.
dgn-np:NP657257.RA5QddsXGStMBA9yCONOqyv68RFNfeJ5GmJhHEG2WSlCY130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP657257.RA5QddsXGStMBA9yCONOqyv68RFNfeJ5GmJhHEG2WSlCY130_assertion
{
miriam-gene:37
a
ncit:C16612
.
lld:C0018801
a
ncit:C7057
.
dgn-gda:DGN742557d6cc4074bb10b1c11f282bfbd8
sio:SIO_000628
miriam-gene:37
,
lld:C0018801
;
a
sio:SIO_001121
.
}
dgn-np:NP657257.RA5QddsXGStMBA9yCONOqyv68RFNfeJ5GmJhHEG2WSlCY130_provenance
{
dgn-np:NP657257.RA5QddsXGStMBA9yCONOqyv68RFNfeJ5GmJhHEG2WSlCY130_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:NP657257.RA5QddsXGStMBA9yCONOqyv68RFNfeJ5GmJhHEG2WSlCY130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:38:35+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" .
}