@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP331045.RAvyc1wfjKKmp4PmZNw8AuiwKRclIn9yoOCi2QwJZMWQQ
> .
@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:NP331045.RAvyc1wfjKKmp4PmZNw8AuiwKRclIn9yoOCi2QwJZMWQQ130_head
{
this:
np:hasAssertion
dgn-np:NP331045.RAvyc1wfjKKmp4PmZNw8AuiwKRclIn9yoOCi2QwJZMWQQ130_assertion
;
np:hasProvenance
dgn-np:NP331045.RAvyc1wfjKKmp4PmZNw8AuiwKRclIn9yoOCi2QwJZMWQQ130_provenance
;
np:hasPublicationInfo
dgn-np:NP331045.RAvyc1wfjKKmp4PmZNw8AuiwKRclIn9yoOCi2QwJZMWQQ130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP331045.RAvyc1wfjKKmp4PmZNw8AuiwKRclIn9yoOCi2QwJZMWQQ130_assertion
a
np:Assertion
.
dgn-np:NP331045.RAvyc1wfjKKmp4PmZNw8AuiwKRclIn9yoOCi2QwJZMWQQ130_provenance
a
np:Provenance
.
dgn-np:NP331045.RAvyc1wfjKKmp4PmZNw8AuiwKRclIn9yoOCi2QwJZMWQQ130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP331045.RAvyc1wfjKKmp4PmZNw8AuiwKRclIn9yoOCi2QwJZMWQQ130_assertion
{
miriam-gene:1756
a
ncit:C16612
.
lld:C0234958
a
ncit:C7057
.
dgn-gda:DGN158c582fe432536ab78543c55069e65f
sio:SIO_000628
miriam-gene:1756
,
lld:C0234958
;
a
sio:SIO_001121
.
}
dgn-np:NP331045.RAvyc1wfjKKmp4PmZNw8AuiwKRclIn9yoOCi2QwJZMWQQ130_provenance
{
dgn-np:NP331045.RAvyc1wfjKKmp4PmZNw8AuiwKRclIn9yoOCi2QwJZMWQQ130_assertion
dcterms:description
"[The absence of skeletal muscle degeneration normally associated with loss of dystrophin function was shown to be due to increased expression of brain (B) and cerebellar Purkinje (CP) isoforms of the gene exclusively in the skeletal muscle of these patients.]. 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:11726549
;
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:NP331045.RAvyc1wfjKKmp4PmZNw8AuiwKRclIn9yoOCi2QwJZMWQQ130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:35:15+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" .
}