@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP174515.RALJLrR1O0mrxKI7OA5hZwqKi9VT7uftxOPrQpMCYCAF4
> .
@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:NP174515.RALJLrR1O0mrxKI7OA5hZwqKi9VT7uftxOPrQpMCYCAF4130_head
{
this:
np:hasAssertion
dgn-np:NP174515.RALJLrR1O0mrxKI7OA5hZwqKi9VT7uftxOPrQpMCYCAF4130_assertion
;
np:hasProvenance
dgn-np:NP174515.RALJLrR1O0mrxKI7OA5hZwqKi9VT7uftxOPrQpMCYCAF4130_provenance
;
np:hasPublicationInfo
dgn-np:NP174515.RALJLrR1O0mrxKI7OA5hZwqKi9VT7uftxOPrQpMCYCAF4130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP174515.RALJLrR1O0mrxKI7OA5hZwqKi9VT7uftxOPrQpMCYCAF4130_assertion
a
np:Assertion
.
dgn-np:NP174515.RALJLrR1O0mrxKI7OA5hZwqKi9VT7uftxOPrQpMCYCAF4130_provenance
a
np:Provenance
.
dgn-np:NP174515.RALJLrR1O0mrxKI7OA5hZwqKi9VT7uftxOPrQpMCYCAF4130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP174515.RALJLrR1O0mrxKI7OA5hZwqKi9VT7uftxOPrQpMCYCAF4130_assertion
{
miriam-gene:1866
a
ncit:C16612
.
lld:C0949445
a
ncit:C7057
.
dgn-gda:DGN7178f92cafc94e9e96910120de13833a
sio:SIO_000628
miriam-gene:1866
,
lld:C0949445
;
a
sio:SIO_001121
.
}
dgn-np:NP174515.RALJLrR1O0mrxKI7OA5hZwqKi9VT7uftxOPrQpMCYCAF4130_provenance
{
dgn-np:NP174515.RALJLrR1O0mrxKI7OA5hZwqKi9VT7uftxOPrQpMCYCAF4130_assertion
dcterms:description
"[The DYT6 locus on chromosome 8 is associated with a mixed phenotype, whereas the DYT7 locus on chromosome 18p is associated with adult onset focal cervical dystonia Several families have been described in which linkage to the known PTD loci have been excluded.]. 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:11261511
;
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:NP174515.RALJLrR1O0mrxKI7OA5hZwqKi9VT7uftxOPrQpMCYCAF4130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:33:34+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" .
}