@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP621085.RA3uGwAeYD64JPOZOre1o-BN9coyONOhsV7ilDu0gY2n4
> .
@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#
> .
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{
this:
np:hasAssertion
dgn-np:NP621085.RA3uGwAeYD64JPOZOre1o-BN9coyONOhsV7ilDu0gY2n4130_assertion
;
np:hasProvenance
dgn-np:NP621085.RA3uGwAeYD64JPOZOre1o-BN9coyONOhsV7ilDu0gY2n4130_provenance
;
np:hasPublicationInfo
dgn-np:NP621085.RA3uGwAeYD64JPOZOre1o-BN9coyONOhsV7ilDu0gY2n4130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP621085.RA3uGwAeYD64JPOZOre1o-BN9coyONOhsV7ilDu0gY2n4130_assertion
a
np:Assertion
.
dgn-np:NP621085.RA3uGwAeYD64JPOZOre1o-BN9coyONOhsV7ilDu0gY2n4130_provenance
a
np:Provenance
.
dgn-np:NP621085.RA3uGwAeYD64JPOZOre1o-BN9coyONOhsV7ilDu0gY2n4130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP621085.RA3uGwAeYD64JPOZOre1o-BN9coyONOhsV7ilDu0gY2n4130_assertion
{
miriam-gene:10020
a
ncit:C16612
.
lld:C0026846
a
ncit:C7057
.
dgn-gda:DGN4ffda5034ceff38a7d542fe38d7c46b9
sio:SIO_000628
miriam-gene:10020
,
lld:C0026846
;
a
sio:SIO_001121
.
}
dgn-np:NP621085.RA3uGwAeYD64JPOZOre1o-BN9coyONOhsV7ilDu0gY2n4130_provenance
{
dgn-np:NP621085.RA3uGwAeYD64JPOZOre1o-BN9coyONOhsV7ilDu0gY2n4130_assertion
dcterms:description
"[In the DMRV/hIBM mouse model, which exhibits hyposialylation in various tissues in addition to muscle atrophy, weakness, and degeneration, we recently have demonstrated that the myopathic phenotype was prevented by oral administration of N-acetylneuraminic acid, N-acetylmannosamine, and sialyllactose, underscoring the crucial role of hyposialylation in the disease pathomechanism.]. 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:22157763
;
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:NP621085.RA3uGwAeYD64JPOZOre1o-BN9coyONOhsV7ilDu0gY2n4130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:38:15+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" .
}