@prefix this: <
http://rdf.disgenet.org/resource/nanopub/NP814750.RAltC_ZA8fp5sc8Luy1TP_DBs5jiUMkQQkLzx7hj9ySDE
> .
@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/
> .
@prefix wi: <
http://purl.org/ontology/wi/core#
> .
@prefix prov: <
http://www.w3.org/ns/prov#
> .
@prefix pav: <
http://purl.org/pav/
> .
@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/resource/nanopub/
> .
@prefix dgn-gda: <
http://rdf.disgenet.org/resource/gda/
> .
@prefix dgn-void: <
http://rdf.disgenet.org/v4.0.0/void/
> .
dgn-np:NP814750.RAltC_ZA8fp5sc8Luy1TP_DBs5jiUMkQQkLzx7hj9ySDE130_head
{
this:
np:hasAssertion
dgn-np:NP814750.RAltC_ZA8fp5sc8Luy1TP_DBs5jiUMkQQkLzx7hj9ySDE130_assertion
;
np:hasProvenance
dgn-np:NP814750.RAltC_ZA8fp5sc8Luy1TP_DBs5jiUMkQQkLzx7hj9ySDE130_provenance
;
np:hasPublicationInfo
dgn-np:NP814750.RAltC_ZA8fp5sc8Luy1TP_DBs5jiUMkQQkLzx7hj9ySDE130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP814750.RAltC_ZA8fp5sc8Luy1TP_DBs5jiUMkQQkLzx7hj9ySDE130_assertion
a
np:Assertion
.
dgn-np:NP814750.RAltC_ZA8fp5sc8Luy1TP_DBs5jiUMkQQkLzx7hj9ySDE130_provenance
a
np:Provenance
.
dgn-np:NP814750.RAltC_ZA8fp5sc8Luy1TP_DBs5jiUMkQQkLzx7hj9ySDE130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP814750.RAltC_ZA8fp5sc8Luy1TP_DBs5jiUMkQQkLzx7hj9ySDE130_assertion
{
miriam-gene:4287
a
ncit:C16612
.
lld:C0024408
a
ncit:C7057
.
dgn-gda:DGN64c52cae82f3fdc060ef28506133a461
sio:SIO_000628
miriam-gene:4287
,
lld:C0024408
;
a
sio:SIO_001121
.
}
dgn-np:NP814750.RAltC_ZA8fp5sc8Luy1TP_DBs5jiUMkQQkLzx7hj9ySDE130_provenance
{
dgn-np:NP814750.RAltC_ZA8fp5sc8Luy1TP_DBs5jiUMkQQkLzx7hj9ySDE130_assertion
dcterms:description
"[Machado-Joseph disease (MJD) is an autosomal dominant neurodegenerative disease caused by an expansion of CAG repeats in the MJD1 gene, in which lower urinary tract dysfunction is known to be the most commonly encountered autonomic failure.]. 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:20503052
;
prov:wasDerivedFrom
dgn-void:befree-2016
;
prov:wasGeneratedBy
eco:ECO_0000203
.
dgn-void:befree-2016
pav:importedOn
"2016-02-19"^^
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:NP814750.RAltC_ZA8fp5sc8Luy1TP_DBs5jiUMkQQkLzx7hj9ySDE130_publicationInfo
{
this:
dcterms:created
"2016-05-13T12:47:54+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:disgenetv3.0rdf
;
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
"v4.0.0.0" .
dgn-void:disgenetv3.0rdf
pav:version
"v4.0.0" .
}