@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP587772.RARq4JJ20y8lpAMQetCl2HZ-3tVTEr4QJYIs2SQtSW3C8
> .
@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:NP587772.RARq4JJ20y8lpAMQetCl2HZ-3tVTEr4QJYIs2SQtSW3C8130_head
{
this:
np:hasAssertion
dgn-np:NP587772.RARq4JJ20y8lpAMQetCl2HZ-3tVTEr4QJYIs2SQtSW3C8130_assertion
;
np:hasProvenance
dgn-np:NP587772.RARq4JJ20y8lpAMQetCl2HZ-3tVTEr4QJYIs2SQtSW3C8130_provenance
;
np:hasPublicationInfo
dgn-np:NP587772.RARq4JJ20y8lpAMQetCl2HZ-3tVTEr4QJYIs2SQtSW3C8130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP587772.RARq4JJ20y8lpAMQetCl2HZ-3tVTEr4QJYIs2SQtSW3C8130_assertion
a
np:Assertion
.
dgn-np:NP587772.RARq4JJ20y8lpAMQetCl2HZ-3tVTEr4QJYIs2SQtSW3C8130_provenance
a
np:Provenance
.
dgn-np:NP587772.RARq4JJ20y8lpAMQetCl2HZ-3tVTEr4QJYIs2SQtSW3C8130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP587772.RARq4JJ20y8lpAMQetCl2HZ-3tVTEr4QJYIs2SQtSW3C8130_assertion
{
miriam-gene:51172
a
ncit:C16612
.
lld:C0038506
a
ncit:C7057
.
dgn-gda:DGNf06a390911082c4fcda104c94654540f
sio:SIO_000628
miriam-gene:51172
,
lld:C0038506
;
a
sio:SIO_001121
.
}
dgn-np:NP587772.RARq4JJ20y8lpAMQetCl2HZ-3tVTEr4QJYIs2SQtSW3C8130_provenance
{
dgn-np:NP587772.RARq4JJ20y8lpAMQetCl2HZ-3tVTEr4QJYIs2SQtSW3C8130_assertion
dcterms:description
"[While data on the GlcNAc-phosphotransferase encoded by GNPTAB/G remains limited and only suggestive, a study of the enzyme encoded by NAGPA has shown that the mutations found in stuttering reduce the overall cellular activity of this enzyme by about half, and that they result in deficits in intracellular processing and trafficking that lead to a reduced cellular half life.]. 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:22884963
;
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:NP587772.RARq4JJ20y8lpAMQetCl2HZ-3tVTEr4QJYIs2SQtSW3C8130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:37:53+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" .
}