@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP618409.RAYY3dgr5x48MlhgBNfHkNeZUxi1L5LTo8tKpZciSUpxo
> .
@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:NP618409.RAYY3dgr5x48MlhgBNfHkNeZUxi1L5LTo8tKpZciSUpxo130_head
{
this:
np:hasAssertion
dgn-np:NP618409.RAYY3dgr5x48MlhgBNfHkNeZUxi1L5LTo8tKpZciSUpxo130_assertion
;
np:hasProvenance
dgn-np:NP618409.RAYY3dgr5x48MlhgBNfHkNeZUxi1L5LTo8tKpZciSUpxo130_provenance
;
np:hasPublicationInfo
dgn-np:NP618409.RAYY3dgr5x48MlhgBNfHkNeZUxi1L5LTo8tKpZciSUpxo130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP618409.RAYY3dgr5x48MlhgBNfHkNeZUxi1L5LTo8tKpZciSUpxo130_assertion
a
np:Assertion
.
dgn-np:NP618409.RAYY3dgr5x48MlhgBNfHkNeZUxi1L5LTo8tKpZciSUpxo130_provenance
a
np:Provenance
.
dgn-np:NP618409.RAYY3dgr5x48MlhgBNfHkNeZUxi1L5LTo8tKpZciSUpxo130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP618409.RAYY3dgr5x48MlhgBNfHkNeZUxi1L5LTo8tKpZciSUpxo130_assertion
{
miriam-gene:367
a
ncit:C16612
.
lld:C0752124
a
ncit:C7057
.
dgn-gda:DGN92d5751af72eebd399e15b9e57fb9d0e
sio:SIO_000628
miriam-gene:367
,
lld:C0752124
;
a
sio:SIO_001121
.
}
dgn-np:NP618409.RAYY3dgr5x48MlhgBNfHkNeZUxi1L5LTo8tKpZciSUpxo130_provenance
{
dgn-np:NP618409.RAYY3dgr5x48MlhgBNfHkNeZUxi1L5LTo8tKpZciSUpxo130_assertion
dcterms:description
"[All the proteins are unrelated outside of the polyglutamine stretch and most are novel with exception of the androgen receptor and the voltage gated alpha 1A calcium channel, which are mutated in spinal and bulbar muscular atrophy and spinocerebellar ataxia type 6.]. 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:9217976
;
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:NP618409.RAYY3dgr5x48MlhgBNfHkNeZUxi1L5LTo8tKpZciSUpxo130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:38:13+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" .
}