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http://rdf.disgenet.org/nanopublications.trig#NP896777.RA-0eEJqzz_wIMPa_BJ5z8onJH6T4U9th5QCgze_V0CK4
> .
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http://www.w3.org/2000/01/rdf-schema#
> .
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http://www.w3.org/2001/XMLSchema#
> .
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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#
> .
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http://rdf.disgenet.org/v2.1.0/void.ttl#
> .
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{
this:
np:hasAssertion
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;
np:hasProvenance
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a
np:Nanopublication
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dgn-np:NP896777.RA-0eEJqzz_wIMPa_BJ5z8onJH6T4U9th5QCgze_V0CK4130_assertion
a
np:Assertion
.
dgn-np:NP896777.RA-0eEJqzz_wIMPa_BJ5z8onJH6T4U9th5QCgze_V0CK4130_provenance
a
np:Provenance
.
dgn-np:NP896777.RA-0eEJqzz_wIMPa_BJ5z8onJH6T4U9th5QCgze_V0CK4130_publicationInfo
a
np:PublicationInfo
.
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{
miriam-gene:120892
a
ncit:C16612
.
lld:C0393571
a
ncit:C7057
.
dgn-gda:DGNe80cb2d17e6c7bda500ece6b6d3dd6cc
sio:SIO_000628
miriam-gene:120892
,
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.
}
dgn-np:NP896777.RA-0eEJqzz_wIMPa_BJ5z8onJH6T4U9th5QCgze_V0CK4130_provenance
{
dgn-np:NP896777.RA-0eEJqzz_wIMPa_BJ5z8onJH6T4U9th5QCgze_V0CK4130_assertion
dcterms:description
"[A total of 458 patients with progressive supranuclear palsy (PSP), multiple system atrophy (MSA), corticobasal ganglionic degeneration (CBGD), atypical Parkinsonism (AP), and LOPD were screened for 14 mutations that span exons 19 to 41 of the LRRK2 gene.]. 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:16602113
;
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:NP896777.RA-0eEJqzz_wIMPa_BJ5z8onJH6T4U9th5QCgze_V0CK4130_publicationInfo
{
this:
dcterms:created
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xsd:dateTime
;
dcterms:rights
<
http://opendatacommons.org/licenses/odbl/1.0/
> ;
dcterms:rightsHolder
dgn-void:IBIGroup
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dcterms:subject
sio:SIO_000983
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prv:usedData
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> , <
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> ;
pav:createdBy
<
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pav:version
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