@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP732384.RA7bBhqHVI17s0fad3djkiWu-SsZuUf5FlEtxLIzvzB3M
> .
@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:NP732384.RA7bBhqHVI17s0fad3djkiWu-SsZuUf5FlEtxLIzvzB3M130_head
{
this:
np:hasAssertion
dgn-np:NP732384.RA7bBhqHVI17s0fad3djkiWu-SsZuUf5FlEtxLIzvzB3M130_assertion
;
np:hasProvenance
dgn-np:NP732384.RA7bBhqHVI17s0fad3djkiWu-SsZuUf5FlEtxLIzvzB3M130_provenance
;
np:hasPublicationInfo
dgn-np:NP732384.RA7bBhqHVI17s0fad3djkiWu-SsZuUf5FlEtxLIzvzB3M130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP732384.RA7bBhqHVI17s0fad3djkiWu-SsZuUf5FlEtxLIzvzB3M130_assertion
a
np:Assertion
.
dgn-np:NP732384.RA7bBhqHVI17s0fad3djkiWu-SsZuUf5FlEtxLIzvzB3M130_provenance
a
np:Provenance
.
dgn-np:NP732384.RA7bBhqHVI17s0fad3djkiWu-SsZuUf5FlEtxLIzvzB3M130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP732384.RA7bBhqHVI17s0fad3djkiWu-SsZuUf5FlEtxLIzvzB3M130_assertion
{
miriam-gene:27335
a
ncit:C16612
.
lld:C0026850
a
ncit:C7057
.
dgn-gda:DGN9b938104df9b63dce90d25e9dc7dd6ea
sio:SIO_000628
miriam-gene:27335
,
lld:C0026850
;
a
sio:SIO_001121
.
}
dgn-np:NP732384.RA7bBhqHVI17s0fad3djkiWu-SsZuUf5FlEtxLIzvzB3M130_provenance
{
dgn-np:NP732384.RA7bBhqHVI17s0fad3djkiWu-SsZuUf5FlEtxLIzvzB3M130_assertion
dcterms:description
"[Both mAbs recognized dystrophin in muscular dystrophy (MD) patients with deletions of exon 3, and further mapping with 11 overlapping synthetic peptides showed that they both recognize an epitope encoded by the muscle-specific exon 1.]. 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:8317478
;
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:NP732384.RA7bBhqHVI17s0fad3djkiWu-SsZuUf5FlEtxLIzvzB3M130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:39:24+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" .
}