@prefix this: <
http://rdf.disgenet.org/resource/nanopub/NP1002301.RAgALSTKdgxQiycUiK3OYr0iUB6_FDgNTbSgjSJgipENM
> .
@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/
> .
@prefix wi: <
http://purl.org/ontology/wi/core#
> .
@prefix prov: <
http://www.w3.org/ns/prov#
> .
@prefix pav: <
http://purl.org/pav/
> .
@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/resource/nanopub/
> .
@prefix dgn-gda: <
http://rdf.disgenet.org/resource/gda/
> .
@prefix dgn-void: <
http://rdf.disgenet.org/v3.0.0/void/
> .
dgn-np:NP1002301.RAgALSTKdgxQiycUiK3OYr0iUB6_FDgNTbSgjSJgipENM130_head
{
this:
np:hasAssertion
dgn-np:NP1002301.RAgALSTKdgxQiycUiK3OYr0iUB6_FDgNTbSgjSJgipENM130_assertion
;
np:hasProvenance
dgn-np:NP1002301.RAgALSTKdgxQiycUiK3OYr0iUB6_FDgNTbSgjSJgipENM130_provenance
;
np:hasPublicationInfo
dgn-np:NP1002301.RAgALSTKdgxQiycUiK3OYr0iUB6_FDgNTbSgjSJgipENM130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP1002301.RAgALSTKdgxQiycUiK3OYr0iUB6_FDgNTbSgjSJgipENM130_assertion
a
np:Assertion
.
dgn-np:NP1002301.RAgALSTKdgxQiycUiK3OYr0iUB6_FDgNTbSgjSJgipENM130_provenance
a
np:Provenance
.
dgn-np:NP1002301.RAgALSTKdgxQiycUiK3OYr0iUB6_FDgNTbSgjSJgipENM130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP1002301.RAgALSTKdgxQiycUiK3OYr0iUB6_FDgNTbSgjSJgipENM130_assertion
{
miriam-gene:493753
a
ncit:C16612
.
lld:C0007194
a
ncit:C7057
.
dgn-gda:DGN7831e4b229f5cbf59936f33e26e7fcd6
sio:SIO_000628
miriam-gene:493753
,
lld:C0007194
;
a
sio:SIO_001121
.
}
dgn-np:NP1002301.RAgALSTKdgxQiycUiK3OYr0iUB6_FDgNTbSgjSJgipENM130_provenance
{
dgn-np:NP1002301.RAgALSTKdgxQiycUiK3OYr0iUB6_FDgNTbSgjSJgipENM130_assertion
dcterms:description
"[The results of this study demonstrate that C2orf64 is essential for human complex IV assembly and that C2orf64 mutational analysis should be considered for complex IV deficient patients, in particular those with hypertrophic cardiomyopathy.]. 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:21457908
;
prov:wasDerivedFrom
dgn-void:befree-20150227
;
prov:wasGeneratedBy
eco:ECO_0000203
.
dgn-void:befree-20150227
pav:importedOn
"2015-02-27"^^
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:NP1002301.RAgALSTKdgxQiycUiK3OYr0iUB6_FDgNTbSgjSJgipENM130_publicationInfo
{
this:
dcterms:created
"2015-08-25T14:48:00+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:disgenetv3.0rdf
;
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
"v3.0.0.0" .
dgn-void:disgenetv3.0rdf
pav:version
"v3.0.0" .
}