@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP846763.RAOu-qDvIcZ55meH42PortesGfCGJa4D3GMeQCIXOOFLo
> .
@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:NP846763.RAOu-qDvIcZ55meH42PortesGfCGJa4D3GMeQCIXOOFLo130_head
{
this:
np:hasAssertion
dgn-np:NP846763.RAOu-qDvIcZ55meH42PortesGfCGJa4D3GMeQCIXOOFLo130_assertion
;
np:hasProvenance
dgn-np:NP846763.RAOu-qDvIcZ55meH42PortesGfCGJa4D3GMeQCIXOOFLo130_provenance
;
np:hasPublicationInfo
dgn-np:NP846763.RAOu-qDvIcZ55meH42PortesGfCGJa4D3GMeQCIXOOFLo130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP846763.RAOu-qDvIcZ55meH42PortesGfCGJa4D3GMeQCIXOOFLo130_assertion
a
np:Assertion
.
dgn-np:NP846763.RAOu-qDvIcZ55meH42PortesGfCGJa4D3GMeQCIXOOFLo130_provenance
a
np:Provenance
.
dgn-np:NP846763.RAOu-qDvIcZ55meH42PortesGfCGJa4D3GMeQCIXOOFLo130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP846763.RAOu-qDvIcZ55meH42PortesGfCGJa4D3GMeQCIXOOFLo130_assertion
{
miriam-gene:1756
a
ncit:C16612
.
lld:C0679466
a
ncit:C7057
.
dgn-gda:DGNc4d0fb99253c11d91f28cd18d14808a2
sio:SIO_000628
miriam-gene:1756
,
lld:C0679466
;
a
sio:SIO_001121
.
}
dgn-np:NP846763.RAOu-qDvIcZ55meH42PortesGfCGJa4D3GMeQCIXOOFLo130_provenance
{
dgn-np:NP846763.RAOu-qDvIcZ55meH42PortesGfCGJa4D3GMeQCIXOOFLo130_assertion
dcterms:description
"[Two decades of molecular, cellular, and functional studies considerably increased our understanding of dystrophins function and unveiled the complex etiology of the cognitive deficits in Duchenne muscular dystrophy (DMD), which involves altered expression of several dystrophin-gene products in brain.]. 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:20625423
;
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:NP846763.RAOu-qDvIcZ55meH42PortesGfCGJa4D3GMeQCIXOOFLo130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:40:37+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
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"v2.1.0" .
}