@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP882000.RA3QwaR9XCckOMNEIGUqleS1iOIk_o2POU_crw3iqDh9c
> .
@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:NP882000.RA3QwaR9XCckOMNEIGUqleS1iOIk_o2POU_crw3iqDh9c130_head
{
this:
np:hasAssertion
dgn-np:NP882000.RA3QwaR9XCckOMNEIGUqleS1iOIk_o2POU_crw3iqDh9c130_assertion
;
np:hasProvenance
dgn-np:NP882000.RA3QwaR9XCckOMNEIGUqleS1iOIk_o2POU_crw3iqDh9c130_provenance
;
np:hasPublicationInfo
dgn-np:NP882000.RA3QwaR9XCckOMNEIGUqleS1iOIk_o2POU_crw3iqDh9c130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP882000.RA3QwaR9XCckOMNEIGUqleS1iOIk_o2POU_crw3iqDh9c130_assertion
a
np:Assertion
.
dgn-np:NP882000.RA3QwaR9XCckOMNEIGUqleS1iOIk_o2POU_crw3iqDh9c130_provenance
a
np:Provenance
.
dgn-np:NP882000.RA3QwaR9XCckOMNEIGUqleS1iOIk_o2POU_crw3iqDh9c130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP882000.RA3QwaR9XCckOMNEIGUqleS1iOIk_o2POU_crw3iqDh9c130_assertion
{
miriam-gene:65018
a
ncit:C16612
.
lld:C0013421
a
ncit:C7057
.
dgn-gda:DGNede2e7b3ab1ac29a9b5de6279d069b70
sio:SIO_000628
miriam-gene:65018
,
lld:C0013421
;
a
sio:SIO_001121
.
}
dgn-np:NP882000.RA3QwaR9XCckOMNEIGUqleS1iOIk_o2POU_crw3iqDh9c130_provenance
{
dgn-np:NP882000.RA3QwaR9XCckOMNEIGUqleS1iOIk_o2POU_crw3iqDh9c130_assertion
dcterms:description
"[The clinical characteristics of 12 PINK1 patients and 114 parkin patients were similar, even for signs such as dystonia at onset and increased reflexes, which were thought to be specific to parkin.]. 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:16401616
;
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:NP882000.RA3QwaR9XCckOMNEIGUqleS1iOIk_o2POU_crw3iqDh9c130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:40:59+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" .
}