@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP897254.RATmCk6Jq1KpRACimYjwNLTEpfLABBHnlKJUaiKYVtxQk
> .
@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:NP897254.RATmCk6Jq1KpRACimYjwNLTEpfLABBHnlKJUaiKYVtxQk130_head
{
this:
np:hasAssertion
dgn-np:NP897254.RATmCk6Jq1KpRACimYjwNLTEpfLABBHnlKJUaiKYVtxQk130_assertion
;
np:hasProvenance
dgn-np:NP897254.RATmCk6Jq1KpRACimYjwNLTEpfLABBHnlKJUaiKYVtxQk130_provenance
;
np:hasPublicationInfo
dgn-np:NP897254.RATmCk6Jq1KpRACimYjwNLTEpfLABBHnlKJUaiKYVtxQk130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP897254.RATmCk6Jq1KpRACimYjwNLTEpfLABBHnlKJUaiKYVtxQk130_assertion
a
np:Assertion
.
dgn-np:NP897254.RATmCk6Jq1KpRACimYjwNLTEpfLABBHnlKJUaiKYVtxQk130_provenance
a
np:Provenance
.
dgn-np:NP897254.RATmCk6Jq1KpRACimYjwNLTEpfLABBHnlKJUaiKYVtxQk130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP897254.RATmCk6Jq1KpRACimYjwNLTEpfLABBHnlKJUaiKYVtxQk130_assertion
{
miriam-gene:1437
a
ncit:C16612
.
lld:C0026650
a
ncit:C7057
.
dgn-gda:DGN58047f8311d97ddded578d4b09c34caa
sio:SIO_000628
miriam-gene:1437
,
lld:C0026650
;
a
sio:SIO_001121
.
}
dgn-np:NP897254.RATmCk6Jq1KpRACimYjwNLTEpfLABBHnlKJUaiKYVtxQk130_provenance
{
dgn-np:NP897254.RATmCk6Jq1KpRACimYjwNLTEpfLABBHnlKJUaiKYVtxQk130_assertion
dcterms:description
"[Rapid-onset dystonia-parkinsonism (RDP) is a genetic movement disorder characterized by abrupt onset over hours to days of bradykinesia, postural instability, dysphagia, dysarthria, and severe dystonic spasms with decreased levels of the dopamine metabolite, homovanillic acid (HVA), in cerebrospinal fluid (CSF).]. 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:9918356
;
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:NP897254.RATmCk6Jq1KpRACimYjwNLTEpfLABBHnlKJUaiKYVtxQk130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:41:11+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" .
}