@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP546286.RAd77KsznEb0E7xbiNnIZ8Z0ccAvU73EzhTt1RWDGcApU
> .
@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 dcterms: <
http://purl.org/dc/terms/
> .
@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:NP546286.RAd77KsznEb0E7xbiNnIZ8Z0ccAvU73EzhTt1RWDGcApU130_head
{
this:
np:hasAssertion
dgn-np:NP546286.RAd77KsznEb0E7xbiNnIZ8Z0ccAvU73EzhTt1RWDGcApU130_assertion
;
np:hasProvenance
dgn-np:NP546286.RAd77KsznEb0E7xbiNnIZ8Z0ccAvU73EzhTt1RWDGcApU130_provenance
;
np:hasPublicationInfo
dgn-np:NP546286.RAd77KsznEb0E7xbiNnIZ8Z0ccAvU73EzhTt1RWDGcApU130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP546286.RAd77KsznEb0E7xbiNnIZ8Z0ccAvU73EzhTt1RWDGcApU130_assertion
a
np:Assertion
.
dgn-np:NP546286.RAd77KsznEb0E7xbiNnIZ8Z0ccAvU73EzhTt1RWDGcApU130_provenance
a
np:Provenance
.
dgn-np:NP546286.RAd77KsznEb0E7xbiNnIZ8Z0ccAvU73EzhTt1RWDGcApU130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP546286.RAd77KsznEb0E7xbiNnIZ8Z0ccAvU73EzhTt1RWDGcApU130_assertion
{
miriam-gene:3736
a
ncit:C16612
.
lld:C1719788
a
ncit:C7057
.
dgn-gda:DGN8c3691f7c4472fbebbdd7d531233db6c
sio:SIO_000628
miriam-gene:3736
,
lld:C1719788
;
a
sio:SIO_001121
.
}
dgn-np:NP546286.RAd77KsznEb0E7xbiNnIZ8Z0ccAvU73EzhTt1RWDGcApU130_provenance
{
dgn-np:NP546286.RAd77KsznEb0E7xbiNnIZ8Z0ccAvU73EzhTt1RWDGcApU130_assertion
dcterms:description
"[Genetic testing for EA1 and EA2 is available, but since no single mutation is prominent for either KCNA1 or CACNA1A, all of the coding regions of the genes need to be screened for mutations.]. 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:21827920
;
prov:wasDerivedFrom
dgn-void:befree-20140225
;
prov:wasGeneratedBy
eco:ECO_0000203
.
dgn-void:befree-20140225
pav:importedOn
"2014-02-25"^^
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:NP546286.RAd77KsznEb0E7xbiNnIZ8Z0ccAvU73EzhTt1RWDGcApU130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:37:29+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: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" .
}