@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP354759.RAAcBTudSMtFgnKaVr7NrBZMvLCQ8cSvuyKog8PNlAcaM
> .
@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:NP354759.RAAcBTudSMtFgnKaVr7NrBZMvLCQ8cSvuyKog8PNlAcaM130_head
{
this:
np:hasAssertion
dgn-np:NP354759.RAAcBTudSMtFgnKaVr7NrBZMvLCQ8cSvuyKog8PNlAcaM130_assertion
;
np:hasProvenance
dgn-np:NP354759.RAAcBTudSMtFgnKaVr7NrBZMvLCQ8cSvuyKog8PNlAcaM130_provenance
;
np:hasPublicationInfo
dgn-np:NP354759.RAAcBTudSMtFgnKaVr7NrBZMvLCQ8cSvuyKog8PNlAcaM130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP354759.RAAcBTudSMtFgnKaVr7NrBZMvLCQ8cSvuyKog8PNlAcaM130_assertion
a
np:Assertion
.
dgn-np:NP354759.RAAcBTudSMtFgnKaVr7NrBZMvLCQ8cSvuyKog8PNlAcaM130_provenance
a
np:Provenance
.
dgn-np:NP354759.RAAcBTudSMtFgnKaVr7NrBZMvLCQ8cSvuyKog8PNlAcaM130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP354759.RAAcBTudSMtFgnKaVr7NrBZMvLCQ8cSvuyKog8PNlAcaM130_assertion
{
miriam-gene:1866
a
ncit:C16612
.
lld:C1394891
a
ncit:C7057
.
dgn-gda:DGNd78782413eedf8375821157d3c60ae9f
sio:SIO_000628
miriam-gene:1866
,
lld:C1394891
;
a
sio:SIO_001121
.
}
dgn-np:NP354759.RAAcBTudSMtFgnKaVr7NrBZMvLCQ8cSvuyKog8PNlAcaM130_provenance
{
dgn-np:NP354759.RAAcBTudSMtFgnKaVr7NrBZMvLCQ8cSvuyKog8PNlAcaM130_assertion
dcterms:description
"[The data also indicate that this dystonia mutation (DYT7) is the predominant cause of IFD, at least in this area of Northwest Germany, and that its location can be narrowed from a 30- to a 6-centimorgan region close to marker D18S1098.]. 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:9225692
;
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:NP354759.RAAcBTudSMtFgnKaVr7NrBZMvLCQ8cSvuyKog8PNlAcaM130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:35:28+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" .
}