@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP216916.RAADZ4c72x8EdXCrlkO0AObq-hJRK4JQrmfRRvn8f1Neo
> .
@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:NP216916.RAADZ4c72x8EdXCrlkO0AObq-hJRK4JQrmfRRvn8f1Neo130_head
{
this:
np:hasAssertion
dgn-np:NP216916.RAADZ4c72x8EdXCrlkO0AObq-hJRK4JQrmfRRvn8f1Neo130_assertion
;
np:hasProvenance
dgn-np:NP216916.RAADZ4c72x8EdXCrlkO0AObq-hJRK4JQrmfRRvn8f1Neo130_provenance
;
np:hasPublicationInfo
dgn-np:NP216916.RAADZ4c72x8EdXCrlkO0AObq-hJRK4JQrmfRRvn8f1Neo130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP216916.RAADZ4c72x8EdXCrlkO0AObq-hJRK4JQrmfRRvn8f1Neo130_assertion
a
np:Assertion
.
dgn-np:NP216916.RAADZ4c72x8EdXCrlkO0AObq-hJRK4JQrmfRRvn8f1Neo130_provenance
a
np:Provenance
.
dgn-np:NP216916.RAADZ4c72x8EdXCrlkO0AObq-hJRK4JQrmfRRvn8f1Neo130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP216916.RAADZ4c72x8EdXCrlkO0AObq-hJRK4JQrmfRRvn8f1Neo130_assertion
{
miriam-gene:2668
a
ncit:C16612
.
lld:C0030567
a
ncit:C7057
.
dgn-gda:DGNab1ee4338dd1f8c514ada70cd5c6e3c8
sio:SIO_000628
miriam-gene:2668
,
lld:C0030567
;
a
sio:SIO_001121
.
}
dgn-np:NP216916.RAADZ4c72x8EdXCrlkO0AObq-hJRK4JQrmfRRvn8f1Neo130_provenance
{
dgn-np:NP216916.RAADZ4c72x8EdXCrlkO0AObq-hJRK4JQrmfRRvn8f1Neo130_assertion
dcterms:description
"[Parkinson's disease is an obvious target for the development of gene therapy procedures which could involve both the delivery of the gene encoding tyrosine hydroxylase to boost dopamine production or the delivery of genes encoding neurotrophic factors such as GDNF to promote the survival of dopaminergic neurons.]. 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:10634236
;
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:NP216916.RAADZ4c72x8EdXCrlkO0AObq-hJRK4JQrmfRRvn8f1Neo130_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" .
}