@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP865923.RA24OqXdl4GwQ-YJaYPFgSLqrv-uZHMs12-N9nOzUqhmg
> .
@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:NP865923.RA24OqXdl4GwQ-YJaYPFgSLqrv-uZHMs12-N9nOzUqhmg130_head
{
this:
np:hasAssertion
dgn-np:NP865923.RA24OqXdl4GwQ-YJaYPFgSLqrv-uZHMs12-N9nOzUqhmg130_assertion
;
np:hasProvenance
dgn-np:NP865923.RA24OqXdl4GwQ-YJaYPFgSLqrv-uZHMs12-N9nOzUqhmg130_provenance
;
np:hasPublicationInfo
dgn-np:NP865923.RA24OqXdl4GwQ-YJaYPFgSLqrv-uZHMs12-N9nOzUqhmg130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP865923.RA24OqXdl4GwQ-YJaYPFgSLqrv-uZHMs12-N9nOzUqhmg130_assertion
a
np:Assertion
.
dgn-np:NP865923.RA24OqXdl4GwQ-YJaYPFgSLqrv-uZHMs12-N9nOzUqhmg130_provenance
a
np:Provenance
.
dgn-np:NP865923.RA24OqXdl4GwQ-YJaYPFgSLqrv-uZHMs12-N9nOzUqhmg130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP865923.RA24OqXdl4GwQ-YJaYPFgSLqrv-uZHMs12-N9nOzUqhmg130_assertion
{
miriam-gene:1433
a
ncit:C16612
.
lld:C1970149
a
ncit:C7057
.
dgn-gda:DGN4892603eef34ffcf8a01c4763a286301
sio:SIO_000628
miriam-gene:1433
,
lld:C1970149
;
a
sio:SIO_001121
.
}
dgn-np:NP865923.RA24OqXdl4GwQ-YJaYPFgSLqrv-uZHMs12-N9nOzUqhmg130_provenance
{
dgn-np:NP865923.RA24OqXdl4GwQ-YJaYPFgSLqrv-uZHMs12-N9nOzUqhmg130_assertion
dcterms:description
"[Three additional autosomal dominant forms (DYT9, DYT19 and DYT20) might exist based on linkage mapping to regions apparently different from, yet in close proximity to or overlapping with the known loci DYT18, DYT10 and DYT8.]. 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:19578124
;
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:NP865923.RA24OqXdl4GwQ-YJaYPFgSLqrv-uZHMs12-N9nOzUqhmg130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:40:49+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" .
}