@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP928756.RAziJm2xxJiNL3nlyRChZ9iP3K5ygSDt79EChjQCWzLKc
> .
@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:NP928756.RAziJm2xxJiNL3nlyRChZ9iP3K5ygSDt79EChjQCWzLKc130_head
{
this:
np:hasAssertion
dgn-np:NP928756.RAziJm2xxJiNL3nlyRChZ9iP3K5ygSDt79EChjQCWzLKc130_assertion
;
np:hasProvenance
dgn-np:NP928756.RAziJm2xxJiNL3nlyRChZ9iP3K5ygSDt79EChjQCWzLKc130_provenance
;
np:hasPublicationInfo
dgn-np:NP928756.RAziJm2xxJiNL3nlyRChZ9iP3K5ygSDt79EChjQCWzLKc130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP928756.RAziJm2xxJiNL3nlyRChZ9iP3K5ygSDt79EChjQCWzLKc130_assertion
a
np:Assertion
.
dgn-np:NP928756.RAziJm2xxJiNL3nlyRChZ9iP3K5ygSDt79EChjQCWzLKc130_provenance
a
np:Provenance
.
dgn-np:NP928756.RAziJm2xxJiNL3nlyRChZ9iP3K5ygSDt79EChjQCWzLKc130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP928756.RAziJm2xxJiNL3nlyRChZ9iP3K5ygSDt79EChjQCWzLKc130_assertion
{
miriam-gene:2395
a
ncit:C16612
.
lld:C0750937
a
ncit:C7057
.
dgn-gda:DGNd70c033c9495813d50345e3a47d83eb3
sio:SIO_000628
miriam-gene:2395
,
lld:C0750937
;
a
sio:SIO_001121
.
}
dgn-np:NP928756.RAziJm2xxJiNL3nlyRChZ9iP3K5ygSDt79EChjQCWzLKc130_provenance
{
dgn-np:NP928756.RAziJm2xxJiNL3nlyRChZ9iP3K5ygSDt79EChjQCWzLKc130_assertion
dcterms:description
"[FXN RNA and protein levels are reduced in patients leading to progressive gait and limb ataxia, sensory loss, reduced tendon reflexes, dysarthria, absent lower limb reflexes, and loss of position and vibration sense.]. 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:22764244
;
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:NP928756.RAziJm2xxJiNL3nlyRChZ9iP3K5ygSDt79EChjQCWzLKc130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:41:29+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" .
}