@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP407630.RAexnD9ZDlFx3oeWiguIFeMc8CKwO2ZtszF_oOv8O1IeE
> .
@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:NP407630.RAexnD9ZDlFx3oeWiguIFeMc8CKwO2ZtszF_oOv8O1IeE130_head
{
this:
np:hasAssertion
dgn-np:NP407630.RAexnD9ZDlFx3oeWiguIFeMc8CKwO2ZtszF_oOv8O1IeE130_assertion
;
np:hasProvenance
dgn-np:NP407630.RAexnD9ZDlFx3oeWiguIFeMc8CKwO2ZtszF_oOv8O1IeE130_provenance
;
np:hasPublicationInfo
dgn-np:NP407630.RAexnD9ZDlFx3oeWiguIFeMc8CKwO2ZtszF_oOv8O1IeE130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP407630.RAexnD9ZDlFx3oeWiguIFeMc8CKwO2ZtszF_oOv8O1IeE130_assertion
a
np:Assertion
.
dgn-np:NP407630.RAexnD9ZDlFx3oeWiguIFeMc8CKwO2ZtszF_oOv8O1IeE130_provenance
a
np:Provenance
.
dgn-np:NP407630.RAexnD9ZDlFx3oeWiguIFeMc8CKwO2ZtszF_oOv8O1IeE130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP407630.RAexnD9ZDlFx3oeWiguIFeMc8CKwO2ZtszF_oOv8O1IeE130_assertion
{
miriam-gene:6310
a
ncit:C16612
.
lld:C0028738
a
ncit:C7057
.
dgn-gda:DGNf9958e8ba3208844ada6288f458ef6fc
sio:SIO_000628
miriam-gene:6310
,
lld:C0028738
;
a
sio:SIO_001121
.
}
dgn-np:NP407630.RAexnD9ZDlFx3oeWiguIFeMc8CKwO2ZtszF_oOv8O1IeE130_provenance
{
dgn-np:NP407630.RAexnD9ZDlFx3oeWiguIFeMc8CKwO2ZtszF_oOv8O1IeE130_assertion
dcterms:description
"[MJD was clinically characterized by a relatively higher frequency of ocular signs such as eyelid retraction, bulging eyes, ophthalmoparesis, and nystagmus, spasticity in lower limbs, and sensory and urinary disturbances in contrast to the SCA1 patients except for slow eye movement.]. 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:8815156
;
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:NP407630.RAexnD9ZDlFx3oeWiguIFeMc8CKwO2ZtszF_oOv8O1IeE130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:36:02+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" .
}