@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP189230.RAWlRyRepDOxcCP-gj6wMMSZAmGQqTn6XTJAaPQUvDfaM
> .
@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:NP189230.RAWlRyRepDOxcCP-gj6wMMSZAmGQqTn6XTJAaPQUvDfaM130_head
{
this:
np:hasAssertion
dgn-np:NP189230.RAWlRyRepDOxcCP-gj6wMMSZAmGQqTn6XTJAaPQUvDfaM130_assertion
;
np:hasProvenance
dgn-np:NP189230.RAWlRyRepDOxcCP-gj6wMMSZAmGQqTn6XTJAaPQUvDfaM130_provenance
;
np:hasPublicationInfo
dgn-np:NP189230.RAWlRyRepDOxcCP-gj6wMMSZAmGQqTn6XTJAaPQUvDfaM130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP189230.RAWlRyRepDOxcCP-gj6wMMSZAmGQqTn6XTJAaPQUvDfaM130_assertion
a
np:Assertion
.
dgn-np:NP189230.RAWlRyRepDOxcCP-gj6wMMSZAmGQqTn6XTJAaPQUvDfaM130_provenance
a
np:Provenance
.
dgn-np:NP189230.RAWlRyRepDOxcCP-gj6wMMSZAmGQqTn6XTJAaPQUvDfaM130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP189230.RAWlRyRepDOxcCP-gj6wMMSZAmGQqTn6XTJAaPQUvDfaM130_assertion
{
miriam-gene:4942
a
ncit:C16612
.
lld:C0456909
a
ncit:C7057
.
dgn-gda:DGNbb0bd903e383b6dabb4346d8c7ff24e1
sio:SIO_000628
miriam-gene:4942
,
lld:C0456909
;
a
sio:SIO_001121
.
}
dgn-np:NP189230.RAWlRyRepDOxcCP-gj6wMMSZAmGQqTn6XTJAaPQUvDfaM130_provenance
{
dgn-np:NP189230.RAWlRyRepDOxcCP-gj6wMMSZAmGQqTn6XTJAaPQUvDfaM130_assertion
dcterms:description
"[A generalized deficiency of the mitochondrial enzyme, ornithine aminotransferase (OAT) is the inborn error in gyrate atrophy, an autosomal recessive degenerative disease of the choroid and retina of the eye that leads to blindness.]. 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:2793865
;
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:NP189230.RAWlRyRepDOxcCP-gj6wMMSZAmGQqTn6XTJAaPQUvDfaM130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:33:44+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" .
}