@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP908642.RAoj-pBukGAE8GdI4urVjKqn3c-xF815KHwns0Y2t1J1o
> .
@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:NP908642.RAoj-pBukGAE8GdI4urVjKqn3c-xF815KHwns0Y2t1J1o130_head
{
this:
np:hasAssertion
dgn-np:NP908642.RAoj-pBukGAE8GdI4urVjKqn3c-xF815KHwns0Y2t1J1o130_assertion
;
np:hasProvenance
dgn-np:NP908642.RAoj-pBukGAE8GdI4urVjKqn3c-xF815KHwns0Y2t1J1o130_provenance
;
np:hasPublicationInfo
dgn-np:NP908642.RAoj-pBukGAE8GdI4urVjKqn3c-xF815KHwns0Y2t1J1o130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP908642.RAoj-pBukGAE8GdI4urVjKqn3c-xF815KHwns0Y2t1J1o130_assertion
a
np:Assertion
.
dgn-np:NP908642.RAoj-pBukGAE8GdI4urVjKqn3c-xF815KHwns0Y2t1J1o130_provenance
a
np:Provenance
.
dgn-np:NP908642.RAoj-pBukGAE8GdI4urVjKqn3c-xF815KHwns0Y2t1J1o130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP908642.RAoj-pBukGAE8GdI4urVjKqn3c-xF815KHwns0Y2t1J1o130_assertion
{
miriam-gene:4574
a
ncit:C16612
.
lld:C0581883
a
ncit:C7057
.
dgn-gda:DGN318f818f3e0d5af303535c5c7e903e75
sio:SIO_000628
miriam-gene:4574
,
lld:C0581883
;
a
sio:SIO_001121
.
}
dgn-np:NP908642.RAoj-pBukGAE8GdI4urVjKqn3c-xF815KHwns0Y2t1J1o130_provenance
{
dgn-np:NP908642.RAoj-pBukGAE8GdI4urVjKqn3c-xF815KHwns0Y2t1J1o130_assertion
dcterms:description
"[Samples from 30 deaf probands exhibiting features suggestive of syndromic mitochondrial deafness or from families with maternal transmission of deafness were selected for investigation of mutations in the mitochondrial genes MT-RNR1 and MT-TS1.]. 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:20722495
;
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:NP908642.RAoj-pBukGAE8GdI4urVjKqn3c-xF815KHwns0Y2t1J1o130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:41:18+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" .
}