@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP492841.RAlurhw5uZXOXs70PPA2lOeV-oPAhVFfq0Q7rbNlEhqK8
> .
@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:NP492841.RAlurhw5uZXOXs70PPA2lOeV-oPAhVFfq0Q7rbNlEhqK8130_head
{
this:
np:hasAssertion
dgn-np:NP492841.RAlurhw5uZXOXs70PPA2lOeV-oPAhVFfq0Q7rbNlEhqK8130_assertion
;
np:hasProvenance
dgn-np:NP492841.RAlurhw5uZXOXs70PPA2lOeV-oPAhVFfq0Q7rbNlEhqK8130_provenance
;
np:hasPublicationInfo
dgn-np:NP492841.RAlurhw5uZXOXs70PPA2lOeV-oPAhVFfq0Q7rbNlEhqK8130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP492841.RAlurhw5uZXOXs70PPA2lOeV-oPAhVFfq0Q7rbNlEhqK8130_assertion
a
np:Assertion
.
dgn-np:NP492841.RAlurhw5uZXOXs70PPA2lOeV-oPAhVFfq0Q7rbNlEhqK8130_provenance
a
np:Provenance
.
dgn-np:NP492841.RAlurhw5uZXOXs70PPA2lOeV-oPAhVFfq0Q7rbNlEhqK8130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP492841.RAlurhw5uZXOXs70PPA2lOeV-oPAhVFfq0Q7rbNlEhqK8130_assertion
{
miriam-gene:6696
a
ncit:C16612
.
lld:C0037019
a
ncit:C7057
.
dgn-gda:DGN40cc9a42c14a12be72c86daa519cfe15
sio:SIO_000628
miriam-gene:6696
,
lld:C0037019
;
a
sio:SIO_001121
.
}
dgn-np:NP492841.RAlurhw5uZXOXs70PPA2lOeV-oPAhVFfq0Q7rbNlEhqK8130_provenance
{
dgn-np:NP492841.RAlurhw5uZXOXs70PPA2lOeV-oPAhVFfq0Q7rbNlEhqK8130_assertion
dcterms:description
"[This was not specific to PD as OPN protein expression was also decreased in the SN in multiple system atrophy and progressive supranuclear palsy with an identical localisation of the protein.]. 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:16962083
;
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:NP492841.RAlurhw5uZXOXs70PPA2lOeV-oPAhVFfq0Q7rbNlEhqK8130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:36:54+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" .
}