@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP879731.RAq5X2ez1r4L_ytzxlqDUpP4vSiQNTt0pSUEhHscl5BaQ
> .
@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:NP879731.RAq5X2ez1r4L_ytzxlqDUpP4vSiQNTt0pSUEhHscl5BaQ130_head
{
this:
np:hasAssertion
dgn-np:NP879731.RAq5X2ez1r4L_ytzxlqDUpP4vSiQNTt0pSUEhHscl5BaQ130_assertion
;
np:hasProvenance
dgn-np:NP879731.RAq5X2ez1r4L_ytzxlqDUpP4vSiQNTt0pSUEhHscl5BaQ130_provenance
;
np:hasPublicationInfo
dgn-np:NP879731.RAq5X2ez1r4L_ytzxlqDUpP4vSiQNTt0pSUEhHscl5BaQ130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP879731.RAq5X2ez1r4L_ytzxlqDUpP4vSiQNTt0pSUEhHscl5BaQ130_assertion
a
np:Assertion
.
dgn-np:NP879731.RAq5X2ez1r4L_ytzxlqDUpP4vSiQNTt0pSUEhHscl5BaQ130_provenance
a
np:Provenance
.
dgn-np:NP879731.RAq5X2ez1r4L_ytzxlqDUpP4vSiQNTt0pSUEhHscl5BaQ130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP879731.RAq5X2ez1r4L_ytzxlqDUpP4vSiQNTt0pSUEhHscl5BaQ130_assertion
{
miriam-gene:2395
a
ncit:C16612
.
lld:C1856689
a
ncit:C7057
.
dgn-gda:DGNb5f38d90d063fbf24eb17c177dd89139
sio:SIO_000628
miriam-gene:2395
,
lld:C1856689
;
a
sio:SIO_001121
.
}
dgn-np:NP879731.RAq5X2ez1r4L_ytzxlqDUpP4vSiQNTt0pSUEhHscl5BaQ130_provenance
{
dgn-np:NP879731.RAq5X2ez1r4L_ytzxlqDUpP4vSiQNTt0pSUEhHscl5BaQ130_assertion
dcterms:description
"[Since the identification of this link, there has been tremendous progress in understanding frataxin function and the mechanism of FRDA pathology, as well as in developing diagnostics and therapeutic approaches for the disease.]. 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:22382366
;
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:NP879731.RAq5X2ez1r4L_ytzxlqDUpP4vSiQNTt0pSUEhHscl5BaQ130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:40:57+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" .
}