@prefix this: <
http://rdf.disgenet.org/resource/nanopub/NP128182.RAdA058hyM8ahS9HCexPceUfRvRTiiI7tQTkN7ysH-cak
> .
@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:NP128182.RAdA058hyM8ahS9HCexPceUfRvRTiiI7tQTkN7ysH-cak130_head
{
this:
np:hasAssertion
dgn-np:NP128182.RAdA058hyM8ahS9HCexPceUfRvRTiiI7tQTkN7ysH-cak130_assertion
;
np:hasProvenance
dgn-np:NP128182.RAdA058hyM8ahS9HCexPceUfRvRTiiI7tQTkN7ysH-cak130_provenance
;
np:hasPublicationInfo
dgn-np:NP128182.RAdA058hyM8ahS9HCexPceUfRvRTiiI7tQTkN7ysH-cak130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP128182.RAdA058hyM8ahS9HCexPceUfRvRTiiI7tQTkN7ysH-cak130_assertion
a
np:Assertion
.
dgn-np:NP128182.RAdA058hyM8ahS9HCexPceUfRvRTiiI7tQTkN7ysH-cak130_provenance
a
np:Provenance
.
dgn-np:NP128182.RAdA058hyM8ahS9HCexPceUfRvRTiiI7tQTkN7ysH-cak130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP128182.RAdA058hyM8ahS9HCexPceUfRvRTiiI7tQTkN7ysH-cak130_assertion
{
miriam-gene:8929
a
ncit:C16612
.
lld:C3203358
a
ncit:C7057
.
dgn-gda:DGNab4c4bf0429abb8a8c494027413b3b43
sio:SIO_000628
miriam-gene:8929
,
lld:C3203358
;
a
sio:SIO_001122
.
}
dgn-np:NP128182.RAdA058hyM8ahS9HCexPceUfRvRTiiI7tQTkN7ysH-cak130_provenance
{
dgn-np:NP128182.RAdA058hyM8ahS9HCexPceUfRvRTiiI7tQTkN7ysH-cak130_assertion
dcterms:description
"[These results confirm a disturbance of cardiac autonomic regulation in CCHS, indicate that PHOX2B genotype is related to the severity of dysregulation, predict the need for cardiac pacemaker, and offer the clinician the potential to avert sudden 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:18041756
;
prov:wasDerivedFrom
dgn-void:gad-20150221
;
prov:wasGeneratedBy
eco:ECO_0000203
.
dgn-void:gad-20150221
pav:importedOn
"2015-02-21"^^
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:NP128182.RAdA058hyM8ahS9HCexPceUfRvRTiiI7tQTkN7ysH-cak130_publicationInfo
{
this:
dcterms:created
"2015-08-25T14:38:52+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" .
}