@prefix dc: <
http://purl.org/dc/terms/
> .
@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP78626.RAoVh8ivQKIGb7aZ-d1p9oZQhWGPrZ0KGhRBzUL0y_3lk
> .
@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 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:NP78626.RAoVh8ivQKIGb7aZ-d1p9oZQhWGPrZ0KGhRBzUL0y_3lk130_head
{
this:
np:hasAssertion
dgn-np:NP78626.RAoVh8ivQKIGb7aZ-d1p9oZQhWGPrZ0KGhRBzUL0y_3lk130_assertion
;
np:hasProvenance
dgn-np:NP78626.RAoVh8ivQKIGb7aZ-d1p9oZQhWGPrZ0KGhRBzUL0y_3lk130_provenance
;
np:hasPublicationInfo
dgn-np:NP78626.RAoVh8ivQKIGb7aZ-d1p9oZQhWGPrZ0KGhRBzUL0y_3lk130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP78626.RAoVh8ivQKIGb7aZ-d1p9oZQhWGPrZ0KGhRBzUL0y_3lk130_assertion
a
np:Assertion
.
dgn-np:NP78626.RAoVh8ivQKIGb7aZ-d1p9oZQhWGPrZ0KGhRBzUL0y_3lk130_provenance
a
np:Provenance
.
dgn-np:NP78626.RAoVh8ivQKIGb7aZ-d1p9oZQhWGPrZ0KGhRBzUL0y_3lk130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP78626.RAoVh8ivQKIGb7aZ-d1p9oZQhWGPrZ0KGhRBzUL0y_3lk130_assertion
{
miriam-gene:9722
a
ncit:C16612
.
lld:C0023976
a
ncit:C7057
.
dgn-gda:DGN5e90bae4e0bbec93e180e701ec0f5f28
sio:SIO_000628
miriam-gene:9722
,
lld:C0023976
;
a
sio:SIO_001122
.
}
dgn-np:NP78626.RAoVh8ivQKIGb7aZ-d1p9oZQhWGPrZ0KGhRBzUL0y_3lk130_provenance
{
dgn-np:NP78626.RAoVh8ivQKIGb7aZ-d1p9oZQhWGPrZ0KGhRBzUL0y_3lk130_assertion
dc:description
"[Subject to confirmation in additional cohorts, we suggest that the NOS1AP tag SNP genotype may provide an additional clinical dimension, which helps assess risk and choice of therapeutic strategies in LQTS.]. 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:20538168
;
prov:wasDerivedFrom
dgn-void:gad-20130706
;
prov:wasGeneratedBy
eco:ECO_0000203
.
dgn-void:gad-20130706
pav:importedOn
"2013-07-06"^^
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:NP78626.RAoVh8ivQKIGb7aZ-d1p9oZQhWGPrZ0KGhRBzUL0y_3lk130_publicationInfo
{
this:
dc:created
"2014-10-02T12:32:38+02:00"^^
xsd:dateTime
;
dc:rights
<
http://opendatacommons.org/licenses/odbl/1.0/
> ;
dc:rightsHolder
dgn-void:IBIGroup
;
dc: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" .
}