@prefix this: <
http://rdf.disgenet.org/resource/nanopub/NP1318916.RAeEWMDjYqqN3tPROK0ZEMv74X_N2cLAyADFD4Zyj-HuY
> .
@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:NP1318916.RAeEWMDjYqqN3tPROK0ZEMv74X_N2cLAyADFD4Zyj-HuY130_head
{
this:
np:hasAssertion
dgn-np:NP1318916.RAeEWMDjYqqN3tPROK0ZEMv74X_N2cLAyADFD4Zyj-HuY130_assertion
;
np:hasProvenance
dgn-np:NP1318916.RAeEWMDjYqqN3tPROK0ZEMv74X_N2cLAyADFD4Zyj-HuY130_provenance
;
np:hasPublicationInfo
dgn-np:NP1318916.RAeEWMDjYqqN3tPROK0ZEMv74X_N2cLAyADFD4Zyj-HuY130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP1318916.RAeEWMDjYqqN3tPROK0ZEMv74X_N2cLAyADFD4Zyj-HuY130_assertion
a
np:Assertion
.
dgn-np:NP1318916.RAeEWMDjYqqN3tPROK0ZEMv74X_N2cLAyADFD4Zyj-HuY130_provenance
a
np:Provenance
.
dgn-np:NP1318916.RAeEWMDjYqqN3tPROK0ZEMv74X_N2cLAyADFD4Zyj-HuY130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP1318916.RAeEWMDjYqqN3tPROK0ZEMv74X_N2cLAyADFD4Zyj-HuY130_assertion
{
miriam-gene:367
a
ncit:C16612
.
lld:C0752353
a
ncit:C7057
.
dgn-gda:DGN69ec06515b9905a874456f81c3f02919
sio:SIO_000628
miriam-gene:367
,
lld:C0752353
;
a
sio:SIO_001121
.
}
dgn-np:NP1318916.RAeEWMDjYqqN3tPROK0ZEMv74X_N2cLAyADFD4Zyj-HuY130_provenance
{
dgn-np:NP1318916.RAeEWMDjYqqN3tPROK0ZEMv74X_N2cLAyADFD4Zyj-HuY130_assertion
dcterms:description
"[An increase in the number of (CAG)n repeats in the first coding exon of the androgen receptor (AR) gene has been strongly associated with Kennedy disease (KD) (spinal and bulbar muscular atrophy).]. 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:7702080
;
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:NP1318916.RAeEWMDjYqqN3tPROK0ZEMv74X_N2cLAyADFD4Zyj-HuY130_publicationInfo
{
this:
dcterms:created
"2016-05-13T12:51:44+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" .
}