@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP216132.RAwyfKZzMRyMmEr2Y1zH2fmEGB9XMpi3uWFW3qYb5p5Z8
> .
@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:NP216132.RAwyfKZzMRyMmEr2Y1zH2fmEGB9XMpi3uWFW3qYb5p5Z8130_head
{
this:
np:hasAssertion
dgn-np:NP216132.RAwyfKZzMRyMmEr2Y1zH2fmEGB9XMpi3uWFW3qYb5p5Z8130_assertion
;
np:hasProvenance
dgn-np:NP216132.RAwyfKZzMRyMmEr2Y1zH2fmEGB9XMpi3uWFW3qYb5p5Z8130_provenance
;
np:hasPublicationInfo
dgn-np:NP216132.RAwyfKZzMRyMmEr2Y1zH2fmEGB9XMpi3uWFW3qYb5p5Z8130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP216132.RAwyfKZzMRyMmEr2Y1zH2fmEGB9XMpi3uWFW3qYb5p5Z8130_assertion
a
np:Assertion
.
dgn-np:NP216132.RAwyfKZzMRyMmEr2Y1zH2fmEGB9XMpi3uWFW3qYb5p5Z8130_provenance
a
np:Provenance
.
dgn-np:NP216132.RAwyfKZzMRyMmEr2Y1zH2fmEGB9XMpi3uWFW3qYb5p5Z8130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP216132.RAwyfKZzMRyMmEr2Y1zH2fmEGB9XMpi3uWFW3qYb5p5Z8130_assertion
{
miriam-gene:51106
a
ncit:C16612
.
lld:C0011053
a
ncit:C7057
.
dgn-gda:DGN7662b99486a422204ab018ba8dee05db
sio:SIO_000628
miriam-gene:51106
,
lld:C0011053
;
a
sio:SIO_001121
.
}
dgn-np:NP216132.RAwyfKZzMRyMmEr2Y1zH2fmEGB9XMpi3uWFW3qYb5p5Z8130_provenance
{
dgn-np:NP216132.RAwyfKZzMRyMmEr2Y1zH2fmEGB9XMpi3uWFW3qYb5p5Z8130_assertion
dcterms:description
"[Since both genes, as well as TFB1M, are involved in the process of mitochondrial RNA modification, it appears that the modification of mitochondrial RNA is an important regulatory pathway in the phenotypic expression of the deafness-associated mitochondrial A1555G mutation.]. 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:15542390
;
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:NP216132.RAwyfKZzMRyMmEr2Y1zH2fmEGB9XMpi3uWFW3qYb5p5Z8130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:34:00+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" .
}