@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP571017.RAE3kkPLYQKbR-Bwvy5EP9NQcac2anTsqC0gN4Lb_OBpo
> .
@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:NP571017.RAE3kkPLYQKbR-Bwvy5EP9NQcac2anTsqC0gN4Lb_OBpo130_head
{
this:
np:hasAssertion
dgn-np:NP571017.RAE3kkPLYQKbR-Bwvy5EP9NQcac2anTsqC0gN4Lb_OBpo130_assertion
;
np:hasProvenance
dgn-np:NP571017.RAE3kkPLYQKbR-Bwvy5EP9NQcac2anTsqC0gN4Lb_OBpo130_provenance
;
np:hasPublicationInfo
dgn-np:NP571017.RAE3kkPLYQKbR-Bwvy5EP9NQcac2anTsqC0gN4Lb_OBpo130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP571017.RAE3kkPLYQKbR-Bwvy5EP9NQcac2anTsqC0gN4Lb_OBpo130_assertion
a
np:Assertion
.
dgn-np:NP571017.RAE3kkPLYQKbR-Bwvy5EP9NQcac2anTsqC0gN4Lb_OBpo130_provenance
a
np:Provenance
.
dgn-np:NP571017.RAE3kkPLYQKbR-Bwvy5EP9NQcac2anTsqC0gN4Lb_OBpo130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP571017.RAE3kkPLYQKbR-Bwvy5EP9NQcac2anTsqC0gN4Lb_OBpo130_assertion
{
miriam-gene:25953
a
ncit:C16612
.
lld:C0026650
a
ncit:C7057
.
dgn-gda:DGN96fbaadf03216dc5e514d9009a9e6d7c
sio:SIO_000628
miriam-gene:25953
,
lld:C0026650
;
a
sio:SIO_001121
.
}
dgn-np:NP571017.RAE3kkPLYQKbR-Bwvy5EP9NQcac2anTsqC0gN4Lb_OBpo130_provenance
{
dgn-np:NP571017.RAE3kkPLYQKbR-Bwvy5EP9NQcac2anTsqC0gN4Lb_OBpo130_assertion
dcterms:description
"[Identifying the PDC locus on chromosome 2q will facilitate discovery of the PDC gene and enable investigators to determine whether PDC is genetically homogeneous and whether other paroxysmal movement disorders are also genetically linked to the PDC locus.]. 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:8659518
;
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:NP571017.RAE3kkPLYQKbR-Bwvy5EP9NQcac2anTsqC0gN4Lb_OBpo130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:37:44+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" .
}