@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP568231.RA8QyI5udGTvDCwXWuHR1UTJH0KC3394SkxC8IVKdd75Y
> .
@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:NP568231.RA8QyI5udGTvDCwXWuHR1UTJH0KC3394SkxC8IVKdd75Y130_head
{
this:
np:hasAssertion
dgn-np:NP568231.RA8QyI5udGTvDCwXWuHR1UTJH0KC3394SkxC8IVKdd75Y130_assertion
;
np:hasProvenance
dgn-np:NP568231.RA8QyI5udGTvDCwXWuHR1UTJH0KC3394SkxC8IVKdd75Y130_provenance
;
np:hasPublicationInfo
dgn-np:NP568231.RA8QyI5udGTvDCwXWuHR1UTJH0KC3394SkxC8IVKdd75Y130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP568231.RA8QyI5udGTvDCwXWuHR1UTJH0KC3394SkxC8IVKdd75Y130_assertion
a
np:Assertion
.
dgn-np:NP568231.RA8QyI5udGTvDCwXWuHR1UTJH0KC3394SkxC8IVKdd75Y130_provenance
a
np:Provenance
.
dgn-np:NP568231.RA8QyI5udGTvDCwXWuHR1UTJH0KC3394SkxC8IVKdd75Y130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP568231.RA8QyI5udGTvDCwXWuHR1UTJH0KC3394SkxC8IVKdd75Y130_assertion
{
miriam-gene:1861
a
ncit:C16612
.
lld:C0154676
a
ncit:C7057
.
dgn-gda:DGN14f352abc9acc23cf8971a19bf85d2ad
sio:SIO_000628
miriam-gene:1861
,
lld:C0154676
;
a
sio:SIO_001121
.
}
dgn-np:NP568231.RA8QyI5udGTvDCwXWuHR1UTJH0KC3394SkxC8IVKdd75Y130_provenance
{
dgn-np:NP568231.RA8QyI5udGTvDCwXWuHR1UTJH0KC3394SkxC8IVKdd75Y130_assertion
dcterms:description
"[Genetic haplotypes at five marker loci that are closely linked to the DYT1 gene on chromosome 9q were determined in 10 Ashkenazi Jewish patients with focal hand dystonia (eight with musician's cramp, two with writer's cramp).]. 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:8684386
;
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:NP568231.RA8QyI5udGTvDCwXWuHR1UTJH0KC3394SkxC8IVKdd75Y130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:37:42+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" .
}