@prefix this: <
http://rdf.disgenet.org/resource/nanopub/NP256188.RANDnrmUMKjksy4xe_BO_awpiw_U6kc0v3DXBDt32ejzY
> .
@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:NP256188.RANDnrmUMKjksy4xe_BO_awpiw_U6kc0v3DXBDt32ejzY130_head
{
this:
np:hasAssertion
dgn-np:NP256188.RANDnrmUMKjksy4xe_BO_awpiw_U6kc0v3DXBDt32ejzY130_assertion
;
np:hasProvenance
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;
np:hasPublicationInfo
dgn-np:NP256188.RANDnrmUMKjksy4xe_BO_awpiw_U6kc0v3DXBDt32ejzY130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP256188.RANDnrmUMKjksy4xe_BO_awpiw_U6kc0v3DXBDt32ejzY130_assertion
a
np:Assertion
.
dgn-np:NP256188.RANDnrmUMKjksy4xe_BO_awpiw_U6kc0v3DXBDt32ejzY130_provenance
a
np:Provenance
.
dgn-np:NP256188.RANDnrmUMKjksy4xe_BO_awpiw_U6kc0v3DXBDt32ejzY130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP256188.RANDnrmUMKjksy4xe_BO_awpiw_U6kc0v3DXBDt32ejzY130_assertion
{
miriam-gene:478
a
ncit:C16612
.
lld:C1868681
a
ncit:C7057
.
dgn-gda:DGN3d373a93b07a15305bdca455bfc9e177
sio:SIO_000628
miriam-gene:478
,
lld:C1868681
;
a
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.
}
dgn-np:NP256188.RANDnrmUMKjksy4xe_BO_awpiw_U6kc0v3DXBDt32ejzY130_provenance
{
dgn-np:NP256188.RANDnrmUMKjksy4xe_BO_awpiw_U6kc0v3DXBDt32ejzY130_assertion
dcterms:description
"[AHC and rapid-onset dystonia-parkinsonism are allelic diseases related to mutations in ATP1A3 and form a phenotypical continuum of a dystonic movement disorder.]. 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:22850527
;
prov:wasDerivedFrom
dgn-void:befree-20150227
;
prov:wasGeneratedBy
eco:ECO_0000203
.
dgn-void:befree-20150227
pav:importedOn
"2015-02-27"^^
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:NP256188.RANDnrmUMKjksy4xe_BO_awpiw_U6kc0v3DXBDt32ejzY130_publicationInfo
{
this:
dcterms:created
"2015-08-25T14:40:05+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
> , <
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> , <
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" .
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pav:version
"v3.0.0" .
}