@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP456118.RAK0atIi6M4F12gSgEfd56sRvPHhGbUghAZsyF5HyHyjs
> .
@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:NP456118.RAK0atIi6M4F12gSgEfd56sRvPHhGbUghAZsyF5HyHyjs130_head
{
this:
np:hasAssertion
dgn-np:NP456118.RAK0atIi6M4F12gSgEfd56sRvPHhGbUghAZsyF5HyHyjs130_assertion
;
np:hasProvenance
dgn-np:NP456118.RAK0atIi6M4F12gSgEfd56sRvPHhGbUghAZsyF5HyHyjs130_provenance
;
np:hasPublicationInfo
dgn-np:NP456118.RAK0atIi6M4F12gSgEfd56sRvPHhGbUghAZsyF5HyHyjs130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP456118.RAK0atIi6M4F12gSgEfd56sRvPHhGbUghAZsyF5HyHyjs130_assertion
a
np:Assertion
.
dgn-np:NP456118.RAK0atIi6M4F12gSgEfd56sRvPHhGbUghAZsyF5HyHyjs130_provenance
a
np:Provenance
.
dgn-np:NP456118.RAK0atIi6M4F12gSgEfd56sRvPHhGbUghAZsyF5HyHyjs130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP456118.RAK0atIi6M4F12gSgEfd56sRvPHhGbUghAZsyF5HyHyjs130_assertion
{
miriam-gene:1861
a
ncit:C16612
.
lld:C0242422
a
ncit:C7057
.
dgn-gda:DGN1ea7285dc91135021ca443b5f5385e12
sio:SIO_000628
miriam-gene:1861
,
lld:C0242422
;
a
sio:SIO_001121
.
}
dgn-np:NP456118.RAK0atIi6M4F12gSgEfd56sRvPHhGbUghAZsyF5HyHyjs130_provenance
{
dgn-np:NP456118.RAK0atIi6M4F12gSgEfd56sRvPHhGbUghAZsyF5HyHyjs130_assertion
dcterms:description
"[Our data suggest that the DYT1 mutation is not associated with significant damage to the nigrostriatal DA system, in keeping with the absence of parkinsonism and levodopa response in this 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:10720299
;
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:NP456118.RAK0atIi6M4F12gSgEfd56sRvPHhGbUghAZsyF5HyHyjs130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:36:32+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" .
}