@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP238147.RAQ_oV7xd0W9E0CuX8gtGHgTTIlxXxOk8iH6zRDOCzxm0
> .
@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:NP238147.RAQ_oV7xd0W9E0CuX8gtGHgTTIlxXxOk8iH6zRDOCzxm0130_head
{
this:
np:hasAssertion
dgn-np:NP238147.RAQ_oV7xd0W9E0CuX8gtGHgTTIlxXxOk8iH6zRDOCzxm0130_assertion
;
np:hasProvenance
dgn-np:NP238147.RAQ_oV7xd0W9E0CuX8gtGHgTTIlxXxOk8iH6zRDOCzxm0130_provenance
;
np:hasPublicationInfo
dgn-np:NP238147.RAQ_oV7xd0W9E0CuX8gtGHgTTIlxXxOk8iH6zRDOCzxm0130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP238147.RAQ_oV7xd0W9E0CuX8gtGHgTTIlxXxOk8iH6zRDOCzxm0130_assertion
a
np:Assertion
.
dgn-np:NP238147.RAQ_oV7xd0W9E0CuX8gtGHgTTIlxXxOk8iH6zRDOCzxm0130_provenance
a
np:Provenance
.
dgn-np:NP238147.RAQ_oV7xd0W9E0CuX8gtGHgTTIlxXxOk8iH6zRDOCzxm0130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP238147.RAQ_oV7xd0W9E0CuX8gtGHgTTIlxXxOk8iH6zRDOCzxm0130_assertion
{
miriam-gene:4538
a
ncit:C16612
.
lld:C0029132
a
ncit:C7057
.
dgn-gda:DGN6ce6a55e71843e7b9eb5d445c862866f
sio:SIO_000628
miriam-gene:4538
,
lld:C0029132
;
a
sio:SIO_001121
.
}
dgn-np:NP238147.RAQ_oV7xd0W9E0CuX8gtGHgTTIlxXxOk8iH6zRDOCzxm0130_provenance
{
dgn-np:NP238147.RAQ_oV7xd0W9E0CuX8gtGHgTTIlxXxOk8iH6zRDOCzxm0130_assertion
dcterms:description
"[It is shown here, however, that neither this biochemical lesion nor the optic neuropathy are due to the mutation at nucleotide position 11,778 of the mitochondrial ND4 gene first identified by Wallace et al.]. 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:2121024
;
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:NP238147.RAQ_oV7xd0W9E0CuX8gtGHgTTIlxXxOk8iH6zRDOCzxm0130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:34:13+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" .
}