@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP799966.RAdpTzfkvcSmnmTONhwfMdyMb5OS6-R7zB8fuizRS8aDA
> .
@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:NP799966.RAdpTzfkvcSmnmTONhwfMdyMb5OS6-R7zB8fuizRS8aDA130_head
{
this:
np:hasAssertion
dgn-np:NP799966.RAdpTzfkvcSmnmTONhwfMdyMb5OS6-R7zB8fuizRS8aDA130_assertion
;
np:hasProvenance
dgn-np:NP799966.RAdpTzfkvcSmnmTONhwfMdyMb5OS6-R7zB8fuizRS8aDA130_provenance
;
np:hasPublicationInfo
dgn-np:NP799966.RAdpTzfkvcSmnmTONhwfMdyMb5OS6-R7zB8fuizRS8aDA130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP799966.RAdpTzfkvcSmnmTONhwfMdyMb5OS6-R7zB8fuizRS8aDA130_assertion
a
np:Assertion
.
dgn-np:NP799966.RAdpTzfkvcSmnmTONhwfMdyMb5OS6-R7zB8fuizRS8aDA130_provenance
a
np:Provenance
.
dgn-np:NP799966.RAdpTzfkvcSmnmTONhwfMdyMb5OS6-R7zB8fuizRS8aDA130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP799966.RAdpTzfkvcSmnmTONhwfMdyMb5OS6-R7zB8fuizRS8aDA130_assertion
{
miriam-gene:1349
a
ncit:C16612
.
lld:C0025958
a
ncit:C7057
.
dgn-gda:DGN995e692930ac8c321a55eed19d5d42fb
sio:SIO_000628
miriam-gene:1349
,
lld:C0025958
;
a
sio:SIO_001121
.
}
dgn-np:NP799966.RAdpTzfkvcSmnmTONhwfMdyMb5OS6-R7zB8fuizRS8aDA130_provenance
{
dgn-np:NP799966.RAdpTzfkvcSmnmTONhwfMdyMb5OS6-R7zB8fuizRS8aDA130_assertion
dcterms:description
"[Downregulation of the COX7B ortholog (cox7B) in medaka (Oryzias latipes) resulted in microcephaly and microphthalmia that recapitulated the MLS phenotype and demonstrated an essential function of complex IV activity in vertebrate CNS development.]. 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:23122588
;
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:NP799966.RAdpTzfkvcSmnmTONhwfMdyMb5OS6-R7zB8fuizRS8aDA130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:40:11+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" .
}