@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP809704.RA_2MTaa3siiIw0vfkKPBQ3pdbcBQywjiUOcn6DpNvPjo
> .
@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:NP809704.RA_2MTaa3siiIw0vfkKPBQ3pdbcBQywjiUOcn6DpNvPjo130_head
{
this:
np:hasAssertion
dgn-np:NP809704.RA_2MTaa3siiIw0vfkKPBQ3pdbcBQywjiUOcn6DpNvPjo130_assertion
;
np:hasProvenance
dgn-np:NP809704.RA_2MTaa3siiIw0vfkKPBQ3pdbcBQywjiUOcn6DpNvPjo130_provenance
;
np:hasPublicationInfo
dgn-np:NP809704.RA_2MTaa3siiIw0vfkKPBQ3pdbcBQywjiUOcn6DpNvPjo130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP809704.RA_2MTaa3siiIw0vfkKPBQ3pdbcBQywjiUOcn6DpNvPjo130_assertion
a
np:Assertion
.
dgn-np:NP809704.RA_2MTaa3siiIw0vfkKPBQ3pdbcBQywjiUOcn6DpNvPjo130_provenance
a
np:Provenance
.
dgn-np:NP809704.RA_2MTaa3siiIw0vfkKPBQ3pdbcBQywjiUOcn6DpNvPjo130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP809704.RA_2MTaa3siiIw0vfkKPBQ3pdbcBQywjiUOcn6DpNvPjo130_assertion
{
miriam-gene:100329167
a
ncit:C16612
.
lld:C0162671
a
ncit:C7057
.
dgn-gda:DGN8375c28e49e21573555a5007c6bfa39e
sio:SIO_000628
miriam-gene:100329167
,
lld:C0162671
;
a
sio:SIO_001121
.
}
dgn-np:NP809704.RA_2MTaa3siiIw0vfkKPBQ3pdbcBQywjiUOcn6DpNvPjo130_provenance
{
dgn-np:NP809704.RA_2MTaa3siiIw0vfkKPBQ3pdbcBQywjiUOcn6DpNvPjo130_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:NP809704.RA_2MTaa3siiIw0vfkKPBQ3pdbcBQywjiUOcn6DpNvPjo130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:40:16+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" .
}