@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP350727.RAuOfyesGH05f7vpez4gjdRO4fPW1ekkXSy0R4VpRy9Sw
> .
@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:NP350727.RAuOfyesGH05f7vpez4gjdRO4fPW1ekkXSy0R4VpRy9Sw130_head
{
this:
np:hasAssertion
dgn-np:NP350727.RAuOfyesGH05f7vpez4gjdRO4fPW1ekkXSy0R4VpRy9Sw130_assertion
;
np:hasProvenance
dgn-np:NP350727.RAuOfyesGH05f7vpez4gjdRO4fPW1ekkXSy0R4VpRy9Sw130_provenance
;
np:hasPublicationInfo
dgn-np:NP350727.RAuOfyesGH05f7vpez4gjdRO4fPW1ekkXSy0R4VpRy9Sw130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP350727.RAuOfyesGH05f7vpez4gjdRO4fPW1ekkXSy0R4VpRy9Sw130_assertion
a
np:Assertion
.
dgn-np:NP350727.RAuOfyesGH05f7vpez4gjdRO4fPW1ekkXSy0R4VpRy9Sw130_provenance
a
np:Provenance
.
dgn-np:NP350727.RAuOfyesGH05f7vpez4gjdRO4fPW1ekkXSy0R4VpRy9Sw130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP350727.RAuOfyesGH05f7vpez4gjdRO4fPW1ekkXSy0R4VpRy9Sw130_assertion
{
miriam-gene:367
a
ncit:C16612
.
lld:C0020179
a
ncit:C7057
.
dgn-gda:DGN1d3d61fb26e0c274aa9d117270e2a7dc
sio:SIO_000628
miriam-gene:367
,
lld:C0020179
;
a
sio:SIO_001121
.
}
dgn-np:NP350727.RAuOfyesGH05f7vpez4gjdRO4fPW1ekkXSy0R4VpRy9Sw130_provenance
{
dgn-np:NP350727.RAuOfyesGH05f7vpez4gjdRO4fPW1ekkXSy0R4VpRy9Sw130_assertion
dcterms:description
"[Lack of significant tissue-specific somatic mosaicism in SBMA including the cerebellar cortex may suggest that CAG repeat expansion in the mutant androgen receptor gene is far more stable compared with that in DRPLA and MJD as well as those reported in Huntington's disease.]. 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:8926495
;
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:NP350727.RAuOfyesGH05f7vpez4gjdRO4fPW1ekkXSy0R4VpRy9Sw130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:35:26+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" .
}