@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP863927.RAvY7tKCDYws2EU1wMb--yEibOJi9AV6ts-UfevtDhROM
> .
@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:NP863927.RAvY7tKCDYws2EU1wMb--yEibOJi9AV6ts-UfevtDhROM130_head
{
this:
np:hasAssertion
dgn-np:NP863927.RAvY7tKCDYws2EU1wMb--yEibOJi9AV6ts-UfevtDhROM130_assertion
;
np:hasProvenance
dgn-np:NP863927.RAvY7tKCDYws2EU1wMb--yEibOJi9AV6ts-UfevtDhROM130_provenance
;
np:hasPublicationInfo
dgn-np:NP863927.RAvY7tKCDYws2EU1wMb--yEibOJi9AV6ts-UfevtDhROM130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP863927.RAvY7tKCDYws2EU1wMb--yEibOJi9AV6ts-UfevtDhROM130_assertion
a
np:Assertion
.
dgn-np:NP863927.RAvY7tKCDYws2EU1wMb--yEibOJi9AV6ts-UfevtDhROM130_provenance
a
np:Provenance
.
dgn-np:NP863927.RAvY7tKCDYws2EU1wMb--yEibOJi9AV6ts-UfevtDhROM130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP863927.RAvY7tKCDYws2EU1wMb--yEibOJi9AV6ts-UfevtDhROM130_assertion
{
miriam-gene:7054
a
ncit:C16612
.
lld:C0035372
a
ncit:C7057
.
dgn-gda:DGNe4cd545cfa8d008c78caa889f8aa5ffb
sio:SIO_000628
miriam-gene:7054
,
lld:C0035372
;
a
sio:SIO_001121
.
}
dgn-np:NP863927.RAvY7tKCDYws2EU1wMb--yEibOJi9AV6ts-UfevtDhROM130_provenance
{
dgn-np:NP863927.RAvY7tKCDYws2EU1wMb--yEibOJi9AV6ts-UfevtDhROM130_assertion
dcterms:description
"[The decrease of tyrosine hydroxylase without neurodegenerative changes observed in the substantia nigra of Rett syndrome had similarity to the pathology caused by excitotoxic lesion of the pedunculopontine nuclei (PPN) observed in an animal experiments.]. 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:11738876
;
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:NP863927.RAvY7tKCDYws2EU1wMb--yEibOJi9AV6ts-UfevtDhROM130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:40:48+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" .
}