@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP917389.RAX9YXFvSO8uxwWqWiQMsjl0bjoKR_WqqkDVDQ3PUb4xM
> .
@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:NP917389.RAX9YXFvSO8uxwWqWiQMsjl0bjoKR_WqqkDVDQ3PUb4xM130_head
{
this:
np:hasAssertion
dgn-np:NP917389.RAX9YXFvSO8uxwWqWiQMsjl0bjoKR_WqqkDVDQ3PUb4xM130_assertion
;
np:hasProvenance
dgn-np:NP917389.RAX9YXFvSO8uxwWqWiQMsjl0bjoKR_WqqkDVDQ3PUb4xM130_provenance
;
np:hasPublicationInfo
dgn-np:NP917389.RAX9YXFvSO8uxwWqWiQMsjl0bjoKR_WqqkDVDQ3PUb4xM130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP917389.RAX9YXFvSO8uxwWqWiQMsjl0bjoKR_WqqkDVDQ3PUb4xM130_assertion
a
np:Assertion
.
dgn-np:NP917389.RAX9YXFvSO8uxwWqWiQMsjl0bjoKR_WqqkDVDQ3PUb4xM130_provenance
a
np:Provenance
.
dgn-np:NP917389.RAX9YXFvSO8uxwWqWiQMsjl0bjoKR_WqqkDVDQ3PUb4xM130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP917389.RAX9YXFvSO8uxwWqWiQMsjl0bjoKR_WqqkDVDQ3PUb4xM130_assertion
{
miriam-gene:4942
a
ncit:C16612
.
lld:C0019247
a
ncit:C7057
.
dgn-gda:DGN6a4bed26073346de19062e62d875eaf4
sio:SIO_000628
miriam-gene:4942
,
lld:C0019247
;
a
sio:SIO_001121
.
}
dgn-np:NP917389.RAX9YXFvSO8uxwWqWiQMsjl0bjoKR_WqqkDVDQ3PUb4xM130_provenance
{
dgn-np:NP917389.RAX9YXFvSO8uxwWqWiQMsjl0bjoKR_WqqkDVDQ3PUb4xM130_assertion
dcterms:description
"[With the final goal of applying gene therapy to this human genetic disease, we have established an in vitro model to test the correction of OAT enzymatic deficiency in mammalian cells, using OAT recombinant retroviruses.]. 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:7712330
;
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:NP917389.RAX9YXFvSO8uxwWqWiQMsjl0bjoKR_WqqkDVDQ3PUb4xM130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:41:23+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" .
}