@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP903942.RArZJ8md8CSQyC-0AkVDA1eClEc7OBQvWV1bRLPilJEG8
> .
@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:NP903942.RArZJ8md8CSQyC-0AkVDA1eClEc7OBQvWV1bRLPilJEG8130_head
{
this:
np:hasAssertion
dgn-np:NP903942.RArZJ8md8CSQyC-0AkVDA1eClEc7OBQvWV1bRLPilJEG8130_assertion
;
np:hasProvenance
dgn-np:NP903942.RArZJ8md8CSQyC-0AkVDA1eClEc7OBQvWV1bRLPilJEG8130_provenance
;
np:hasPublicationInfo
dgn-np:NP903942.RArZJ8md8CSQyC-0AkVDA1eClEc7OBQvWV1bRLPilJEG8130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP903942.RArZJ8md8CSQyC-0AkVDA1eClEc7OBQvWV1bRLPilJEG8130_assertion
a
np:Assertion
.
dgn-np:NP903942.RArZJ8md8CSQyC-0AkVDA1eClEc7OBQvWV1bRLPilJEG8130_provenance
a
np:Provenance
.
dgn-np:NP903942.RArZJ8md8CSQyC-0AkVDA1eClEc7OBQvWV1bRLPilJEG8130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP903942.RArZJ8md8CSQyC-0AkVDA1eClEc7OBQvWV1bRLPilJEG8130_assertion
{
miriam-gene:367
a
ncit:C16612
.
lld:C0393547
a
ncit:C7057
.
dgn-gda:DGNe4bc6ccf7e5342fa65285ded1f493c2f
sio:SIO_000628
miriam-gene:367
,
lld:C0393547
;
a
sio:SIO_001121
.
}
dgn-np:NP903942.RArZJ8md8CSQyC-0AkVDA1eClEc7OBQvWV1bRLPilJEG8130_provenance
{
dgn-np:NP903942.RArZJ8md8CSQyC-0AkVDA1eClEc7OBQvWV1bRLPilJEG8130_assertion
dcterms:description
"[The recent identification of a mutation of the androgen receptor gene in Kennedy's disease or X-linked bulbospinal neuronopathy, a rare form of progressive lower motor neurone degeneration, also associated with clinical signs of androgen insensitivity, raises the possibility that androgen function may be disturbed in other motor neurone disorders, including ALS.]. 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:8400860
;
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:NP903942.RArZJ8md8CSQyC-0AkVDA1eClEc7OBQvWV1bRLPilJEG8130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:41:15+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" .
}