@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP858144.RAu1S74FSO-Qc6_VLjlhoZQ9H1yj3wt08zws4TX2p-ca4
> .
@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:NP858144.RAu1S74FSO-Qc6_VLjlhoZQ9H1yj3wt08zws4TX2p-ca4130_head
{
this:
np:hasAssertion
dgn-np:NP858144.RAu1S74FSO-Qc6_VLjlhoZQ9H1yj3wt08zws4TX2p-ca4130_assertion
;
np:hasProvenance
dgn-np:NP858144.RAu1S74FSO-Qc6_VLjlhoZQ9H1yj3wt08zws4TX2p-ca4130_provenance
;
np:hasPublicationInfo
dgn-np:NP858144.RAu1S74FSO-Qc6_VLjlhoZQ9H1yj3wt08zws4TX2p-ca4130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP858144.RAu1S74FSO-Qc6_VLjlhoZQ9H1yj3wt08zws4TX2p-ca4130_assertion
a
np:Assertion
.
dgn-np:NP858144.RAu1S74FSO-Qc6_VLjlhoZQ9H1yj3wt08zws4TX2p-ca4130_provenance
a
np:Provenance
.
dgn-np:NP858144.RAu1S74FSO-Qc6_VLjlhoZQ9H1yj3wt08zws4TX2p-ca4130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP858144.RAu1S74FSO-Qc6_VLjlhoZQ9H1yj3wt08zws4TX2p-ca4130_assertion
{
miriam-gene:1861
a
ncit:C16612
.
lld:C0338902
a
ncit:C7057
.
dgn-gda:DGN7e405b514e398bc0d837c5294951ecc9
sio:SIO_000628
miriam-gene:1861
,
lld:C0338902
;
a
sio:SIO_001121
.
}
dgn-np:NP858144.RAu1S74FSO-Qc6_VLjlhoZQ9H1yj3wt08zws4TX2p-ca4130_provenance
{
dgn-np:NP858144.RAu1S74FSO-Qc6_VLjlhoZQ9H1yj3wt08zws4TX2p-ca4130_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:NP858144.RAu1S74FSO-Qc6_VLjlhoZQ9H1yj3wt08zws4TX2p-ca4130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:40:44+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" .
}