@prefix this: <
http://rdf.disgenet.org/resource/nanopub/NP394301.RAlcMzDXukuECY7OHjgR9Dtt8bOKWMwmt3FimhH6B60OE
> .
@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/v4.0.0/void/
> .
dgn-np:NP394301.RAlcMzDXukuECY7OHjgR9Dtt8bOKWMwmt3FimhH6B60OE130_head
{
this:
np:hasAssertion
dgn-np:NP394301.RAlcMzDXukuECY7OHjgR9Dtt8bOKWMwmt3FimhH6B60OE130_assertion
;
np:hasProvenance
dgn-np:NP394301.RAlcMzDXukuECY7OHjgR9Dtt8bOKWMwmt3FimhH6B60OE130_provenance
;
np:hasPublicationInfo
dgn-np:NP394301.RAlcMzDXukuECY7OHjgR9Dtt8bOKWMwmt3FimhH6B60OE130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP394301.RAlcMzDXukuECY7OHjgR9Dtt8bOKWMwmt3FimhH6B60OE130_assertion
a
np:Assertion
.
dgn-np:NP394301.RAlcMzDXukuECY7OHjgR9Dtt8bOKWMwmt3FimhH6B60OE130_provenance
a
np:Provenance
.
dgn-np:NP394301.RAlcMzDXukuECY7OHjgR9Dtt8bOKWMwmt3FimhH6B60OE130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP394301.RAlcMzDXukuECY7OHjgR9Dtt8bOKWMwmt3FimhH6B60OE130_assertion
{
miriam-gene:6331
a
ncit:C16612
.
lld:C0023976
a
ncit:C7057
.
dgn-gda:DGN4108455b96bf4e48a90b3f40859f0f60
sio:SIO_000628
miriam-gene:6331
,
lld:C0023976
;
a
sio:SIO_001121
.
}
dgn-np:NP394301.RAlcMzDXukuECY7OHjgR9Dtt8bOKWMwmt3FimhH6B60OE130_provenance
{
dgn-np:NP394301.RAlcMzDXukuECY7OHjgR9Dtt8bOKWMwmt3FimhH6B60OE130_assertion
dcterms:description
"[In the last few years, a very active line of research took place after the first identification of SCN5A mutations associated with an inherited form of cardiac arrhythmias and sudden death, the LQT3 variant of the long QT syndrome.]. 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:12747584
;
prov:wasDerivedFrom
dgn-void:befree-2016
;
prov:wasGeneratedBy
eco:ECO_0000203
.
dgn-void:befree-2016
pav:importedOn
"2016-02-19"^^
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:NP394301.RAlcMzDXukuECY7OHjgR9Dtt8bOKWMwmt3FimhH6B60OE130_publicationInfo
{
this:
dcterms:created
"2016-05-13T12:44:44+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
"v4.0.0.0" .
dgn-void:disgenetv3.0rdf
pav:version
"v4.0.0" .
}