@prefix this: <
http://rdf.disgenet.org/resource/nanopub/NP78772.RA3Fz2Xbgi0kwVnTNQmPtpuqU0EOBWGoXF1Ixwi094NJw
> .
@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:NP78772.RA3Fz2Xbgi0kwVnTNQmPtpuqU0EOBWGoXF1Ixwi094NJw130_head
{
this:
np:hasAssertion
dgn-np:NP78772.RA3Fz2Xbgi0kwVnTNQmPtpuqU0EOBWGoXF1Ixwi094NJw130_assertion
;
np:hasProvenance
dgn-np:NP78772.RA3Fz2Xbgi0kwVnTNQmPtpuqU0EOBWGoXF1Ixwi094NJw130_provenance
;
np:hasPublicationInfo
dgn-np:NP78772.RA3Fz2Xbgi0kwVnTNQmPtpuqU0EOBWGoXF1Ixwi094NJw130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP78772.RA3Fz2Xbgi0kwVnTNQmPtpuqU0EOBWGoXF1Ixwi094NJw130_assertion
a
np:Assertion
.
dgn-np:NP78772.RA3Fz2Xbgi0kwVnTNQmPtpuqU0EOBWGoXF1Ixwi094NJw130_provenance
a
np:Provenance
.
dgn-np:NP78772.RA3Fz2Xbgi0kwVnTNQmPtpuqU0EOBWGoXF1Ixwi094NJw130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP78772.RA3Fz2Xbgi0kwVnTNQmPtpuqU0EOBWGoXF1Ixwi094NJw130_assertion
{
miriam-gene:3753
a
ncit:C16612
.
lld:C0522055
a
ncit:C7057
.
dgn-gda:DGNa9b3743e92dd4b456e7ab7f277deac5c
sio:SIO_000628
miriam-gene:3753
,
lld:C0522055
;
a
sio:SIO_001122
.
}
dgn-np:NP78772.RA3Fz2Xbgi0kwVnTNQmPtpuqU0EOBWGoXF1Ixwi094NJw130_provenance
{
dgn-np:NP78772.RA3Fz2Xbgi0kwVnTNQmPtpuqU0EOBWGoXF1Ixwi094NJw130_assertion
dcterms:description
"[ In this comprehensive cardiac channel gene screen of the largest cohort of consecutive, unrelated patients referred for LQTS genetic testing, half of the patients had an identifiable mutation. The majority of mutations continue to represent novel singlet]. 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:15840476
;
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:NP78772.RA3Fz2Xbgi0kwVnTNQmPtpuqU0EOBWGoXF1Ixwi094NJw130_publicationInfo
{
this:
dcterms:created
"2015-08-25T14:38:23+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" .
}