@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP510778.RAccVM6Y7tTifQlITgHL8IFa0qXMrITnQYJnhZf0j1n6s
> .
@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:NP510778.RAccVM6Y7tTifQlITgHL8IFa0qXMrITnQYJnhZf0j1n6s130_head
{
this:
np:hasAssertion
dgn-np:NP510778.RAccVM6Y7tTifQlITgHL8IFa0qXMrITnQYJnhZf0j1n6s130_assertion
;
np:hasProvenance
dgn-np:NP510778.RAccVM6Y7tTifQlITgHL8IFa0qXMrITnQYJnhZf0j1n6s130_provenance
;
np:hasPublicationInfo
dgn-np:NP510778.RAccVM6Y7tTifQlITgHL8IFa0qXMrITnQYJnhZf0j1n6s130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP510778.RAccVM6Y7tTifQlITgHL8IFa0qXMrITnQYJnhZf0j1n6s130_assertion
a
np:Assertion
.
dgn-np:NP510778.RAccVM6Y7tTifQlITgHL8IFa0qXMrITnQYJnhZf0j1n6s130_provenance
a
np:Provenance
.
dgn-np:NP510778.RAccVM6Y7tTifQlITgHL8IFa0qXMrITnQYJnhZf0j1n6s130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP510778.RAccVM6Y7tTifQlITgHL8IFa0qXMrITnQYJnhZf0j1n6s130_assertion
{
miriam-gene:4397
a
ncit:C16612
.
lld:C0030567
a
ncit:C7057
.
dgn-gda:DGN2f9a84627ee1821f6981b9e72e621a20
sio:SIO_000628
miriam-gene:4397
,
lld:C0030567
;
a
sio:SIO_001121
.
}
dgn-np:NP510778.RAccVM6Y7tTifQlITgHL8IFa0qXMrITnQYJnhZf0j1n6s130_provenance
{
dgn-np:NP510778.RAccVM6Y7tTifQlITgHL8IFa0qXMrITnQYJnhZf0j1n6s130_assertion
dcterms:description
"[There is not currently evidence for shared causation or pathogenesis between the two neurological disorders but we will follow with interest the emerging genetic characterization of parkin in both PD and MS.]. 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:22523156
;
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:NP510778.RAccVM6Y7tTifQlITgHL8IFa0qXMrITnQYJnhZf0j1n6s130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:37:04+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" .
}