@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP660461.RApV2c_6rPTBJy5EEe5o96d8coWN4o-yhHogX-00_N94s
> .
@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:NP660461.RApV2c_6rPTBJy5EEe5o96d8coWN4o-yhHogX-00_N94s130_head
{
this:
np:hasAssertion
dgn-np:NP660461.RApV2c_6rPTBJy5EEe5o96d8coWN4o-yhHogX-00_N94s130_assertion
;
np:hasProvenance
dgn-np:NP660461.RApV2c_6rPTBJy5EEe5o96d8coWN4o-yhHogX-00_N94s130_provenance
;
np:hasPublicationInfo
dgn-np:NP660461.RApV2c_6rPTBJy5EEe5o96d8coWN4o-yhHogX-00_N94s130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP660461.RApV2c_6rPTBJy5EEe5o96d8coWN4o-yhHogX-00_N94s130_assertion
a
np:Assertion
.
dgn-np:NP660461.RApV2c_6rPTBJy5EEe5o96d8coWN4o-yhHogX-00_N94s130_provenance
a
np:Provenance
.
dgn-np:NP660461.RApV2c_6rPTBJy5EEe5o96d8coWN4o-yhHogX-00_N94s130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP660461.RApV2c_6rPTBJy5EEe5o96d8coWN4o-yhHogX-00_N94s130_assertion
{
miriam-gene:4908
a
ncit:C16612
.
lld:C0030567
a
ncit:C7057
.
dgn-gda:DGNdeda8cd1258939bc8d33e6795001e7dd
sio:SIO_000628
miriam-gene:4908
,
lld:C0030567
;
a
sio:SIO_001121
.
}
dgn-np:NP660461.RApV2c_6rPTBJy5EEe5o96d8coWN4o-yhHogX-00_N94s130_provenance
{
dgn-np:NP660461.RApV2c_6rPTBJy5EEe5o96d8coWN4o-yhHogX-00_N94s130_assertion
dcterms:description
"[Neurturin (NTN) is a neurotrophic factor with known potential to protect and restore the function of dopaminergic substantia nigra neurons whose degeneration has been most closely linked to the major motor deficits in Parkinson's disease (PD).]. 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:17532642
;
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:NP660461.RApV2c_6rPTBJy5EEe5o96d8coWN4o-yhHogX-00_N94s130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:38:39+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" .
}