@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP493850.RAmj9QmzFxtwKc0nq7q2CzI3JAsy_haStCfm3gXG31dfU
> .
@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:NP493850.RAmj9QmzFxtwKc0nq7q2CzI3JAsy_haStCfm3gXG31dfU130_head
{
this:
np:hasAssertion
dgn-np:NP493850.RAmj9QmzFxtwKc0nq7q2CzI3JAsy_haStCfm3gXG31dfU130_assertion
;
np:hasProvenance
dgn-np:NP493850.RAmj9QmzFxtwKc0nq7q2CzI3JAsy_haStCfm3gXG31dfU130_provenance
;
np:hasPublicationInfo
dgn-np:NP493850.RAmj9QmzFxtwKc0nq7q2CzI3JAsy_haStCfm3gXG31dfU130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP493850.RAmj9QmzFxtwKc0nq7q2CzI3JAsy_haStCfm3gXG31dfU130_assertion
a
np:Assertion
.
dgn-np:NP493850.RAmj9QmzFxtwKc0nq7q2CzI3JAsy_haStCfm3gXG31dfU130_provenance
a
np:Provenance
.
dgn-np:NP493850.RAmj9QmzFxtwKc0nq7q2CzI3JAsy_haStCfm3gXG31dfU130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP493850.RAmj9QmzFxtwKc0nq7q2CzI3JAsy_haStCfm3gXG31dfU130_assertion
{
miriam-gene:9997
a
ncit:C16612
.
lld:C0268237
a
ncit:C7057
.
dgn-gda:DGN92f199448a308355b4e9a319dd0d664e
sio:SIO_000628
miriam-gene:9997
,
lld:C0268237
;
a
sio:SIO_001121
.
}
dgn-np:NP493850.RAmj9QmzFxtwKc0nq7q2CzI3JAsy_haStCfm3gXG31dfU130_provenance
{
dgn-np:NP493850.RAmj9QmzFxtwKc0nq7q2CzI3JAsy_haStCfm3gXG31dfU130_assertion
dcterms:description
"[Our data demonstrate that the COX deficiency observed in fibroblasts, myoblasts and myotubes from patients with SCO2 mutations can be restored to almost normal levels by the addition of CuCl(2) to the growth medium.]. 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:11931660
;
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:NP493850.RAmj9QmzFxtwKc0nq7q2CzI3JAsy_haStCfm3gXG31dfU130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:36:55+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" .
}