@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP194764.RAd7H3ZPJGQAPjR16cnESA77no4JfpEUFFyFz7I4rKZvk
> .
@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:NP194764.RAd7H3ZPJGQAPjR16cnESA77no4JfpEUFFyFz7I4rKZvk130_head
{
this:
np:hasAssertion
dgn-np:NP194764.RAd7H3ZPJGQAPjR16cnESA77no4JfpEUFFyFz7I4rKZvk130_assertion
;
np:hasProvenance
dgn-np:NP194764.RAd7H3ZPJGQAPjR16cnESA77no4JfpEUFFyFz7I4rKZvk130_provenance
;
np:hasPublicationInfo
dgn-np:NP194764.RAd7H3ZPJGQAPjR16cnESA77no4JfpEUFFyFz7I4rKZvk130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP194764.RAd7H3ZPJGQAPjR16cnESA77no4JfpEUFFyFz7I4rKZvk130_assertion
a
np:Assertion
.
dgn-np:NP194764.RAd7H3ZPJGQAPjR16cnESA77no4JfpEUFFyFz7I4rKZvk130_provenance
a
np:Provenance
.
dgn-np:NP194764.RAd7H3ZPJGQAPjR16cnESA77no4JfpEUFFyFz7I4rKZvk130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP194764.RAd7H3ZPJGQAPjR16cnESA77no4JfpEUFFyFz7I4rKZvk130_assertion
{
miriam-gene:120892
a
ncit:C16612
.
lld:C0085400
a
ncit:C7057
.
dgn-gda:DGNe985533ed1a492204e5aa2c6d177a8e6
sio:SIO_000628
miriam-gene:120892
,
lld:C0085400
;
a
sio:SIO_001121
.
}
dgn-np:NP194764.RAd7H3ZPJGQAPjR16cnESA77no4JfpEUFFyFz7I4rKZvk130_provenance
{
dgn-np:NP194764.RAd7H3ZPJGQAPjR16cnESA77no4JfpEUFFyFz7I4rKZvk130_assertion
dcterms:description
"[Understanding the molecular function of the LRRK2 protein and its associated pathways might elucidate the switch between Lewy body pathology and neurofibrillary tangles, and holds promise for prospective therapeutics that might slow or halt progression of many forms of parkinsonism.]. 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:16406842
;
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:NP194764.RAd7H3ZPJGQAPjR16cnESA77no4JfpEUFFyFz7I4rKZvk130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:33:47+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" .
}