@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP592625.RAvSn48PAV3q1rzlxrKSH4dhKOZPDg3GG63VyHr30i9fE
> .
@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:NP592625.RAvSn48PAV3q1rzlxrKSH4dhKOZPDg3GG63VyHr30i9fE130_head
{
this:
np:hasAssertion
dgn-np:NP592625.RAvSn48PAV3q1rzlxrKSH4dhKOZPDg3GG63VyHr30i9fE130_assertion
;
np:hasProvenance
dgn-np:NP592625.RAvSn48PAV3q1rzlxrKSH4dhKOZPDg3GG63VyHr30i9fE130_provenance
;
np:hasPublicationInfo
dgn-np:NP592625.RAvSn48PAV3q1rzlxrKSH4dhKOZPDg3GG63VyHr30i9fE130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP592625.RAvSn48PAV3q1rzlxrKSH4dhKOZPDg3GG63VyHr30i9fE130_assertion
a
np:Assertion
.
dgn-np:NP592625.RAvSn48PAV3q1rzlxrKSH4dhKOZPDg3GG63VyHr30i9fE130_provenance
a
np:Provenance
.
dgn-np:NP592625.RAvSn48PAV3q1rzlxrKSH4dhKOZPDg3GG63VyHr30i9fE130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP592625.RAvSn48PAV3q1rzlxrKSH4dhKOZPDg3GG63VyHr30i9fE130_assertion
{
miriam-gene:1644
a
ncit:C16612
.
lld:C0030567
a
ncit:C7057
.
dgn-gda:DGNd3421f4b606d19edad4b57344fa38992
sio:SIO_000628
miriam-gene:1644
,
lld:C0030567
;
a
sio:SIO_001121
.
}
dgn-np:NP592625.RAvSn48PAV3q1rzlxrKSH4dhKOZPDg3GG63VyHr30i9fE130_provenance
{
dgn-np:NP592625.RAvSn48PAV3q1rzlxrKSH4dhKOZPDg3GG63VyHr30i9fE130_assertion
dcterms:description
"[Now, we have developed a simple, fast, and reliable method to assay the activities of TH and AADC and have provided the possibility of ex vivo gene therapy for PD by genetically modifying cells with separate hTH, hGCH1, and hAADC genes.]. 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:16338639
;
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:NP592625.RAvSn48PAV3q1rzlxrKSH4dhKOZPDg3GG63VyHr30i9fE130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:37:56+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" .
}