@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP2435.RAK9LoSeyO7wQVmUmvtN1tMVngntuejOBJTfOugNrlis4
> .
@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:NP2435.RAK9LoSeyO7wQVmUmvtN1tMVngntuejOBJTfOugNrlis4130_head
{
this:
np:hasAssertion
dgn-np:NP2435.RAK9LoSeyO7wQVmUmvtN1tMVngntuejOBJTfOugNrlis4130_assertion
;
np:hasProvenance
dgn-np:NP2435.RAK9LoSeyO7wQVmUmvtN1tMVngntuejOBJTfOugNrlis4130_provenance
;
np:hasPublicationInfo
dgn-np:NP2435.RAK9LoSeyO7wQVmUmvtN1tMVngntuejOBJTfOugNrlis4130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP2435.RAK9LoSeyO7wQVmUmvtN1tMVngntuejOBJTfOugNrlis4130_assertion
a
np:Assertion
.
dgn-np:NP2435.RAK9LoSeyO7wQVmUmvtN1tMVngntuejOBJTfOugNrlis4130_provenance
a
np:Provenance
.
dgn-np:NP2435.RAK9LoSeyO7wQVmUmvtN1tMVngntuejOBJTfOugNrlis4130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP2435.RAK9LoSeyO7wQVmUmvtN1tMVngntuejOBJTfOugNrlis4130_assertion
{
miriam-gene:2395
a
ncit:C16612
.
lld:C1856689
a
ncit:C7057
.
dgn-gda:DGN33f7a1430203a66252441abd5f86eccf
sio:SIO_000628
miriam-gene:2395
,
lld:C1856689
;
a
sio:SIO_001122
.
}
dgn-np:NP2435.RAK9LoSeyO7wQVmUmvtN1tMVngntuejOBJTfOugNrlis4130_provenance
{
dgn-np:NP2435.RAK9LoSeyO7wQVmUmvtN1tMVngntuejOBJTfOugNrlis4130_assertion
dcterms:description
"[These new cellular models, which are the first to spontaneously reproduce all the biochemical phenotypes associated with FRDA, are important tools to gain new insights into the in vivo consequences of pathological missense mutations as well as for large-scale pharmacological screening aimed at compensating frataxin deficiency.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine."@en ;
wi:evidence
dgn-void:source_evidence_curated
;
sio:SIO_000772
miriam-pubmed:19629184
;
prov:wasDerivedFrom
dgn-void:uniprot-20130724
;
prov:wasGeneratedBy
eco:ECO_0000218
.
dgn-void:source_evidence_curated
a
eco:ECO_0000205
;
rdfs:comment
"Gene-disease associations manually curated."@en ;
rdfs:label
"DisGeNET evidence - CURATED"@en .
dgn-void:uniprot-20130724
pav:importedOn
"2013-07-24"^^
xsd:date
.
}
dgn-np:NP2435.RAK9LoSeyO7wQVmUmvtN1tMVngntuejOBJTfOugNrlis4130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:31:59+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" .
}