@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP740895.RA8YnIBnH8Cg3Vna1G6Ziob60ZMfDiCUsdfBMTvSuzsB8
> .
@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:NP740895.RA8YnIBnH8Cg3Vna1G6Ziob60ZMfDiCUsdfBMTvSuzsB8130_head
{
this:
np:hasAssertion
dgn-np:NP740895.RA8YnIBnH8Cg3Vna1G6Ziob60ZMfDiCUsdfBMTvSuzsB8130_assertion
;
np:hasProvenance
dgn-np:NP740895.RA8YnIBnH8Cg3Vna1G6Ziob60ZMfDiCUsdfBMTvSuzsB8130_provenance
;
np:hasPublicationInfo
dgn-np:NP740895.RA8YnIBnH8Cg3Vna1G6Ziob60ZMfDiCUsdfBMTvSuzsB8130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP740895.RA8YnIBnH8Cg3Vna1G6Ziob60ZMfDiCUsdfBMTvSuzsB8130_assertion
a
np:Assertion
.
dgn-np:NP740895.RA8YnIBnH8Cg3Vna1G6Ziob60ZMfDiCUsdfBMTvSuzsB8130_provenance
a
np:Provenance
.
dgn-np:NP740895.RA8YnIBnH8Cg3Vna1G6Ziob60ZMfDiCUsdfBMTvSuzsB8130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP740895.RA8YnIBnH8Cg3Vna1G6Ziob60ZMfDiCUsdfBMTvSuzsB8130_assertion
{
miriam-gene:80025
a
ncit:C16612
.
lld:C0030567
a
ncit:C7057
.
dgn-gda:DGN0970978b803c008872c142d9b5ac1131
sio:SIO_000628
miriam-gene:80025
,
lld:C0030567
;
a
sio:SIO_001121
.
}
dgn-np:NP740895.RA8YnIBnH8Cg3Vna1G6Ziob60ZMfDiCUsdfBMTvSuzsB8130_provenance
{
dgn-np:NP740895.RA8YnIBnH8Cg3Vna1G6Ziob60ZMfDiCUsdfBMTvSuzsB8130_assertion
dcterms:description
"[These include prevalent conditions such as Parkinson's disease (PD), dementia with Lewy bodies (DLB), and the Lewy body variant of Alzheimer's disease (LBVAD), as well as rarer conditions including multiple systems atrophy (MSA), and neurodegeneration with brain iron accumulation type-1 (NBIA-1).]. 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:12814657
;
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:NP740895.RA8YnIBnH8Cg3Vna1G6Ziob60ZMfDiCUsdfBMTvSuzsB8130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:39:29+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" .
}