@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP278110.RA43LGBnt3G_uPa1qOYe9IZyUawqm3vlqXjEqUMAe3M8k
> .
@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:NP278110.RA43LGBnt3G_uPa1qOYe9IZyUawqm3vlqXjEqUMAe3M8k130_head
{
this:
np:hasAssertion
dgn-np:NP278110.RA43LGBnt3G_uPa1qOYe9IZyUawqm3vlqXjEqUMAe3M8k130_assertion
;
np:hasProvenance
dgn-np:NP278110.RA43LGBnt3G_uPa1qOYe9IZyUawqm3vlqXjEqUMAe3M8k130_provenance
;
np:hasPublicationInfo
dgn-np:NP278110.RA43LGBnt3G_uPa1qOYe9IZyUawqm3vlqXjEqUMAe3M8k130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP278110.RA43LGBnt3G_uPa1qOYe9IZyUawqm3vlqXjEqUMAe3M8k130_assertion
a
np:Assertion
.
dgn-np:NP278110.RA43LGBnt3G_uPa1qOYe9IZyUawqm3vlqXjEqUMAe3M8k130_provenance
a
np:Provenance
.
dgn-np:NP278110.RA43LGBnt3G_uPa1qOYe9IZyUawqm3vlqXjEqUMAe3M8k130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP278110.RA43LGBnt3G_uPa1qOYe9IZyUawqm3vlqXjEqUMAe3M8k130_assertion
{
miriam-gene:4287
a
ncit:C16612
.
lld:C1839259
a
ncit:C7057
.
dgn-gda:DGN428428fea21c427d00cd19628472b11a
sio:SIO_000628
miriam-gene:4287
,
lld:C1839259
;
a
sio:SIO_001121
.
}
dgn-np:NP278110.RA43LGBnt3G_uPa1qOYe9IZyUawqm3vlqXjEqUMAe3M8k130_provenance
{
dgn-np:NP278110.RA43LGBnt3G_uPa1qOYe9IZyUawqm3vlqXjEqUMAe3M8k130_assertion
dcterms:description
"[The size of CAG repeats in the AR gene is one of the determinant factors of the severity and progression rate of SBMA phenotypes, but the meiotic and somatic instability of CAG repeats is far more stable as compared with other diseases caused by trinucleotide repeat expansions such as HD, DRPLA, MJD and SCA1.]. 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:8725492
;
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:NP278110.RA43LGBnt3G_uPa1qOYe9IZyUawqm3vlqXjEqUMAe3M8k130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:34:37+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" .
}