@prefix this: <
http://rdf.disgenet.org/resource/nanopub/NP537341.RA0-Nmw-R95V_sAaizvtseC-03nsTOcYyy_bcL4KXLKh0
> .
@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:NP537341.RA0-Nmw-R95V_sAaizvtseC-03nsTOcYyy_bcL4KXLKh0130_head
{
this:
np:hasAssertion
dgn-np:NP537341.RA0-Nmw-R95V_sAaizvtseC-03nsTOcYyy_bcL4KXLKh0130_assertion
;
np:hasProvenance
dgn-np:NP537341.RA0-Nmw-R95V_sAaizvtseC-03nsTOcYyy_bcL4KXLKh0130_provenance
;
np:hasPublicationInfo
dgn-np:NP537341.RA0-Nmw-R95V_sAaizvtseC-03nsTOcYyy_bcL4KXLKh0130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP537341.RA0-Nmw-R95V_sAaizvtseC-03nsTOcYyy_bcL4KXLKh0130_assertion
a
np:Assertion
.
dgn-np:NP537341.RA0-Nmw-R95V_sAaizvtseC-03nsTOcYyy_bcL4KXLKh0130_provenance
a
np:Provenance
.
dgn-np:NP537341.RA0-Nmw-R95V_sAaizvtseC-03nsTOcYyy_bcL4KXLKh0130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP537341.RA0-Nmw-R95V_sAaizvtseC-03nsTOcYyy_bcL4KXLKh0130_assertion
{
miriam-gene:3759
a
ncit:C16612
.
lld:C0030443
a
ncit:C7057
.
dgn-gda:DGN37a4ccf36d3adfa5b1ff9c057bb0ac58
sio:SIO_000628
miriam-gene:3759
,
lld:C0030443
;
a
sio:SIO_001121
.
}
dgn-np:NP537341.RA0-Nmw-R95V_sAaizvtseC-03nsTOcYyy_bcL4KXLKh0130_provenance
{
dgn-np:NP537341.RA0-Nmw-R95V_sAaizvtseC-03nsTOcYyy_bcL4KXLKh0130_assertion
dcterms:description
"[Andersen-Tawil syndrome, a skeletal muscle syndrome associated with periodic paralysis and long QT intervals on the ECG, has been linked to defects in KCNJ2, the gene encoding for the inward rectifier potassium channel (I(K1).]. 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:16500306
;
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:NP537341.RA0-Nmw-R95V_sAaizvtseC-03nsTOcYyy_bcL4KXLKh0130_publicationInfo
{
this:
dcterms:created
"2016-05-13T12:45:48+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" .
}