@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP759102.RAkMUz3cTv6UavkKTsuJbCk5HyZCfIvRUzQMJPhWWlyGo
> .
@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:NP759102.RAkMUz3cTv6UavkKTsuJbCk5HyZCfIvRUzQMJPhWWlyGo130_head
{
this:
np:hasAssertion
dgn-np:NP759102.RAkMUz3cTv6UavkKTsuJbCk5HyZCfIvRUzQMJPhWWlyGo130_assertion
;
np:hasProvenance
dgn-np:NP759102.RAkMUz3cTv6UavkKTsuJbCk5HyZCfIvRUzQMJPhWWlyGo130_provenance
;
np:hasPublicationInfo
dgn-np:NP759102.RAkMUz3cTv6UavkKTsuJbCk5HyZCfIvRUzQMJPhWWlyGo130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP759102.RAkMUz3cTv6UavkKTsuJbCk5HyZCfIvRUzQMJPhWWlyGo130_assertion
a
np:Assertion
.
dgn-np:NP759102.RAkMUz3cTv6UavkKTsuJbCk5HyZCfIvRUzQMJPhWWlyGo130_provenance
a
np:Provenance
.
dgn-np:NP759102.RAkMUz3cTv6UavkKTsuJbCk5HyZCfIvRUzQMJPhWWlyGo130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP759102.RAkMUz3cTv6UavkKTsuJbCk5HyZCfIvRUzQMJPhWWlyGo130_assertion
{
miriam-gene:351
a
ncit:C16612
.
lld:C0162671
a
ncit:C7057
.
dgn-gda:DGN5fc45cd4c985e640d4b381012d7c65e4
sio:SIO_000628
miriam-gene:351
,
lld:C0162671
;
a
sio:SIO_001121
.
}
dgn-np:NP759102.RAkMUz3cTv6UavkKTsuJbCk5HyZCfIvRUzQMJPhWWlyGo130_provenance
{
dgn-np:NP759102.RAkMUz3cTv6UavkKTsuJbCk5HyZCfIvRUzQMJPhWWlyGo130_assertion
dcterms:description
"[The MERRF mt tRNA(Lys) lacking the wobble modification cannot translate either of its codons (AAA and AAG), while the translational activity of MELAS mt tRNA(Leu(UUR)) lacking wobble modification is more depressed in decoding of UUG codon than UUA codon.]. 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:17132941
;
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:NP759102.RAkMUz3cTv6UavkKTsuJbCk5HyZCfIvRUzQMJPhWWlyGo130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:39:39+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" .
}