@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP491051.RAOJGElB6gKQgg-9i6ug3u218oYm0bVEO3RpKZmbJStpE
> .
@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:NP491051.RAOJGElB6gKQgg-9i6ug3u218oYm0bVEO3RpKZmbJStpE130_head
{
this:
np:hasAssertion
dgn-np:NP491051.RAOJGElB6gKQgg-9i6ug3u218oYm0bVEO3RpKZmbJStpE130_assertion
;
np:hasProvenance
dgn-np:NP491051.RAOJGElB6gKQgg-9i6ug3u218oYm0bVEO3RpKZmbJStpE130_provenance
;
np:hasPublicationInfo
dgn-np:NP491051.RAOJGElB6gKQgg-9i6ug3u218oYm0bVEO3RpKZmbJStpE130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP491051.RAOJGElB6gKQgg-9i6ug3u218oYm0bVEO3RpKZmbJStpE130_assertion
a
np:Assertion
.
dgn-np:NP491051.RAOJGElB6gKQgg-9i6ug3u218oYm0bVEO3RpKZmbJStpE130_provenance
a
np:Provenance
.
dgn-np:NP491051.RAOJGElB6gKQgg-9i6ug3u218oYm0bVEO3RpKZmbJStpE130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP491051.RAOJGElB6gKQgg-9i6ug3u218oYm0bVEO3RpKZmbJStpE130_assertion
{
miriam-gene:2643
a
ncit:C16612
.
lld:C0242422
a
ncit:C7057
.
dgn-gda:DGN178d6f03590d25a2d111f796cbf1ba71
sio:SIO_000628
miriam-gene:2643
,
lld:C0242422
;
a
sio:SIO_001121
.
}
dgn-np:NP491051.RAOJGElB6gKQgg-9i6ug3u218oYm0bVEO3RpKZmbJStpE130_provenance
{
dgn-np:NP491051.RAOJGElB6gKQgg-9i6ug3u218oYm0bVEO3RpKZmbJStpE130_assertion
dcterms:description
"[Dopa-responsive dystonia (DRD), also known as Segawa syndrome or hereditary progressive dystonia with diurnal fluctuation, is clinically characterized by the occurrence of simultaneous or late Parkinsonism and by an excellent response to treatment with low doses of L-dopa.]. 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:18752196
;
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:NP491051.RAOJGElB6gKQgg-9i6ug3u218oYm0bVEO3RpKZmbJStpE130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:36:53+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" .
}