@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP363770.RAxIJ07zAhtd_w3YYV6nvAAu8OmIgE32rBeS6U2jTmOjE
> .
@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:NP363770.RAxIJ07zAhtd_w3YYV6nvAAu8OmIgE32rBeS6U2jTmOjE130_head
{
this:
np:hasAssertion
dgn-np:NP363770.RAxIJ07zAhtd_w3YYV6nvAAu8OmIgE32rBeS6U2jTmOjE130_assertion
;
np:hasProvenance
dgn-np:NP363770.RAxIJ07zAhtd_w3YYV6nvAAu8OmIgE32rBeS6U2jTmOjE130_provenance
;
np:hasPublicationInfo
dgn-np:NP363770.RAxIJ07zAhtd_w3YYV6nvAAu8OmIgE32rBeS6U2jTmOjE130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP363770.RAxIJ07zAhtd_w3YYV6nvAAu8OmIgE32rBeS6U2jTmOjE130_assertion
a
np:Assertion
.
dgn-np:NP363770.RAxIJ07zAhtd_w3YYV6nvAAu8OmIgE32rBeS6U2jTmOjE130_provenance
a
np:Provenance
.
dgn-np:NP363770.RAxIJ07zAhtd_w3YYV6nvAAu8OmIgE32rBeS6U2jTmOjE130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP363770.RAxIJ07zAhtd_w3YYV6nvAAu8OmIgE32rBeS6U2jTmOjE130_assertion
{
miriam-gene:2395
a
ncit:C16612
.
lld:C0278134
a
ncit:C7057
.
dgn-gda:DGNbaff9e95c6463953d0bdeba0f299e4e0
sio:SIO_000628
miriam-gene:2395
,
lld:C0278134
;
a
sio:SIO_001121
.
}
dgn-np:NP363770.RAxIJ07zAhtd_w3YYV6nvAAu8OmIgE32rBeS6U2jTmOjE130_provenance
{
dgn-np:NP363770.RAxIJ07zAhtd_w3YYV6nvAAu8OmIgE32rBeS6U2jTmOjE130_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:NP363770.RAxIJ07zAhtd_w3YYV6nvAAu8OmIgE32rBeS6U2jTmOjE130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:35:33+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" .
}