@prefix this: <
http://rdf.disgenet.org/resource/nanopub/NP534730.RA8mnE1NbcIFrq6YD1DMHKhmICcCJAIhh7GC48NtO6Oh4
> .
@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/
> .
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{
this:
np:hasAssertion
dgn-np:NP534730.RA8mnE1NbcIFrq6YD1DMHKhmICcCJAIhh7GC48NtO6Oh4130_assertion
;
np:hasProvenance
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np:hasPublicationInfo
dgn-np:NP534730.RA8mnE1NbcIFrq6YD1DMHKhmICcCJAIhh7GC48NtO6Oh4130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP534730.RA8mnE1NbcIFrq6YD1DMHKhmICcCJAIhh7GC48NtO6Oh4130_assertion
a
np:Assertion
.
dgn-np:NP534730.RA8mnE1NbcIFrq6YD1DMHKhmICcCJAIhh7GC48NtO6Oh4130_provenance
a
np:Provenance
.
dgn-np:NP534730.RA8mnE1NbcIFrq6YD1DMHKhmICcCJAIhh7GC48NtO6Oh4130_publicationInfo
a
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.
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{
miriam-gene:3753
a
ncit:C16612
.
lld:C0023976
a
ncit:C7057
.
dgn-gda:DGN2c6a5bf40f01e1ef30ce9d9c0aa6353d
sio:SIO_000628
miriam-gene:3753
,
lld:C0023976
;
a
sio:SIO_001121
.
}
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{
dgn-np:NP534730.RA8mnE1NbcIFrq6YD1DMHKhmICcCJAIhh7GC48NtO6Oh4130_assertion
dcterms:description
"[Data on the Jervell and Lange-Nielsen syndrome (J-LN), the long-QT syndrome (LQTS) variant associated with deafness and caused by homozygous or compound heterozygous mutations on the KCNQ1 or on the KCNE1 genes encoding the I(Ks) current, are still based largely on case reports.]. 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:16461811
;
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 .
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dgn-np:NP534730.RA8mnE1NbcIFrq6YD1DMHKhmICcCJAIhh7GC48NtO6Oh4130_publicationInfo
{
this:
dcterms:created
"2016-05-13T12:45:47+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
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;
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" .
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pav:version
"v4.0.0" .
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