@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP216316.RA-EDAPR79o8hrDbjGB01jhSXmoVi8bMfNOQn0G0llNVI
> .
@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:NP216316.RA-EDAPR79o8hrDbjGB01jhSXmoVi8bMfNOQn0G0llNVI130_head
{
this:
np:hasAssertion
dgn-np:NP216316.RA-EDAPR79o8hrDbjGB01jhSXmoVi8bMfNOQn0G0llNVI130_assertion
;
np:hasProvenance
dgn-np:NP216316.RA-EDAPR79o8hrDbjGB01jhSXmoVi8bMfNOQn0G0llNVI130_provenance
;
np:hasPublicationInfo
dgn-np:NP216316.RA-EDAPR79o8hrDbjGB01jhSXmoVi8bMfNOQn0G0llNVI130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP216316.RA-EDAPR79o8hrDbjGB01jhSXmoVi8bMfNOQn0G0llNVI130_assertion
a
np:Assertion
.
dgn-np:NP216316.RA-EDAPR79o8hrDbjGB01jhSXmoVi8bMfNOQn0G0llNVI130_provenance
a
np:Provenance
.
dgn-np:NP216316.RA-EDAPR79o8hrDbjGB01jhSXmoVi8bMfNOQn0G0llNVI130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP216316.RA-EDAPR79o8hrDbjGB01jhSXmoVi8bMfNOQn0G0llNVI130_assertion
{
miriam-gene:6696
a
ncit:C16612
.
lld:C0038868
a
ncit:C7057
.
dgn-gda:DGN4b8240425941196c8cdc52b8d44d16c1
sio:SIO_000628
miriam-gene:6696
,
lld:C0038868
;
a
sio:SIO_001121
.
}
dgn-np:NP216316.RA-EDAPR79o8hrDbjGB01jhSXmoVi8bMfNOQn0G0llNVI130_provenance
{
dgn-np:NP216316.RA-EDAPR79o8hrDbjGB01jhSXmoVi8bMfNOQn0G0llNVI130_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:NP216316.RA-EDAPR79o8hrDbjGB01jhSXmoVi8bMfNOQn0G0llNVI130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:34:00+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" .
}