@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP918572.RA7XX_O-vZOhykDtHLorI76kAt-M_D9SGAzPqMnzmd5QQ
> .
@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:NP918572.RA7XX_O-vZOhykDtHLorI76kAt-M_D9SGAzPqMnzmd5QQ130_head
{
this:
np:hasAssertion
dgn-np:NP918572.RA7XX_O-vZOhykDtHLorI76kAt-M_D9SGAzPqMnzmd5QQ130_assertion
;
np:hasProvenance
dgn-np:NP918572.RA7XX_O-vZOhykDtHLorI76kAt-M_D9SGAzPqMnzmd5QQ130_provenance
;
np:hasPublicationInfo
dgn-np:NP918572.RA7XX_O-vZOhykDtHLorI76kAt-M_D9SGAzPqMnzmd5QQ130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP918572.RA7XX_O-vZOhykDtHLorI76kAt-M_D9SGAzPqMnzmd5QQ130_assertion
a
np:Assertion
.
dgn-np:NP918572.RA7XX_O-vZOhykDtHLorI76kAt-M_D9SGAzPqMnzmd5QQ130_provenance
a
np:Provenance
.
dgn-np:NP918572.RA7XX_O-vZOhykDtHLorI76kAt-M_D9SGAzPqMnzmd5QQ130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP918572.RA7XX_O-vZOhykDtHLorI76kAt-M_D9SGAzPqMnzmd5QQ130_assertion
{
miriam-gene:1861
a
ncit:C16612
.
lld:C0743332
a
ncit:C7057
.
dgn-gda:DGN8ff9dfd9e82ece3edf6529bd64a62568
sio:SIO_000628
miriam-gene:1861
,
lld:C0743332
;
a
sio:SIO_001121
.
}
dgn-np:NP918572.RA7XX_O-vZOhykDtHLorI76kAt-M_D9SGAzPqMnzmd5QQ130_provenance
{
dgn-np:NP918572.RA7XX_O-vZOhykDtHLorI76kAt-M_D9SGAzPqMnzmd5QQ130_assertion
dcterms:description
"[Taken together, these results suggest that most cases of focal dystonia in patients of northern German or central European origin are due neither to the GAG deletion in DYT1 nor to a proposed founder mutation on chromosome 18p but must be caused by other genetic or environmental factors.]. 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:9837831
;
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:NP918572.RA7XX_O-vZOhykDtHLorI76kAt-M_D9SGAzPqMnzmd5QQ130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:41:23+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" .
}