@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP381528.RAG4nzSaT1pcYJw3XxmnFlhtrZhLJ3zqG7Gnyq4q35YOw
> .
@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:NP381528.RAG4nzSaT1pcYJw3XxmnFlhtrZhLJ3zqG7Gnyq4q35YOw130_head
{
this:
np:hasAssertion
dgn-np:NP381528.RAG4nzSaT1pcYJw3XxmnFlhtrZhLJ3zqG7Gnyq4q35YOw130_assertion
;
np:hasProvenance
dgn-np:NP381528.RAG4nzSaT1pcYJw3XxmnFlhtrZhLJ3zqG7Gnyq4q35YOw130_provenance
;
np:hasPublicationInfo
dgn-np:NP381528.RAG4nzSaT1pcYJw3XxmnFlhtrZhLJ3zqG7Gnyq4q35YOw130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP381528.RAG4nzSaT1pcYJw3XxmnFlhtrZhLJ3zqG7Gnyq4q35YOw130_assertion
a
np:Assertion
.
dgn-np:NP381528.RAG4nzSaT1pcYJw3XxmnFlhtrZhLJ3zqG7Gnyq4q35YOw130_provenance
a
np:Provenance
.
dgn-np:NP381528.RAG4nzSaT1pcYJw3XxmnFlhtrZhLJ3zqG7Gnyq4q35YOw130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP381528.RAG4nzSaT1pcYJw3XxmnFlhtrZhLJ3zqG7Gnyq4q35YOw130_assertion
{
miriam-gene:4942
a
ncit:C16612
.
lld:C0018425
a
ncit:C7057
.
dgn-gda:DGN9e008ac6dc2f3e3fc5956af73e17d045
sio:SIO_000628
miriam-gene:4942
,
lld:C0018425
;
a
sio:SIO_001121
.
}
dgn-np:NP381528.RAG4nzSaT1pcYJw3XxmnFlhtrZhLJ3zqG7Gnyq4q35YOw130_provenance
{
dgn-np:NP381528.RAG4nzSaT1pcYJw3XxmnFlhtrZhLJ3zqG7Gnyq4q35YOw130_assertion
dcterms:description
"[A generalized biochemical deficiency of the mitochondrial matrix enzyme ornithine aminotransferase (OAT) is the inborn error in gyrate atrophy (GA), an autosomal recessive blinding disease of the retina and choroid of the eye.]. 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:8125717
;
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:NP381528.RAG4nzSaT1pcYJw3XxmnFlhtrZhLJ3zqG7Gnyq4q35YOw130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:35:45+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" .
}