@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP154827.RA2jMqwiLZISIwURM5KLtJOnTp741bJLUz466QdZAWUJI
> .
@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:NP154827.RA2jMqwiLZISIwURM5KLtJOnTp741bJLUz466QdZAWUJI130_head
{
this:
np:hasAssertion
dgn-np:NP154827.RA2jMqwiLZISIwURM5KLtJOnTp741bJLUz466QdZAWUJI130_assertion
;
np:hasProvenance
dgn-np:NP154827.RA2jMqwiLZISIwURM5KLtJOnTp741bJLUz466QdZAWUJI130_provenance
;
np:hasPublicationInfo
dgn-np:NP154827.RA2jMqwiLZISIwURM5KLtJOnTp741bJLUz466QdZAWUJI130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP154827.RA2jMqwiLZISIwURM5KLtJOnTp741bJLUz466QdZAWUJI130_assertion
a
np:Assertion
.
dgn-np:NP154827.RA2jMqwiLZISIwURM5KLtJOnTp741bJLUz466QdZAWUJI130_provenance
a
np:Provenance
.
dgn-np:NP154827.RA2jMqwiLZISIwURM5KLtJOnTp741bJLUz466QdZAWUJI130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP154827.RA2jMqwiLZISIwURM5KLtJOnTp741bJLUz466QdZAWUJI130_assertion
{
miriam-gene:1756
a
ncit:C16612
.
lld:C0013264
a
ncit:C7057
.
dgn-gda:DGN932585718db22ce1f5b12f8883612a7a
sio:SIO_000628
miriam-gene:1756
,
lld:C0013264
;
a
sio:SIO_001121
.
}
dgn-np:NP154827.RA2jMqwiLZISIwURM5KLtJOnTp741bJLUz466QdZAWUJI130_provenance
{
dgn-np:NP154827.RA2jMqwiLZISIwURM5KLtJOnTp741bJLUz466QdZAWUJI130_assertion
dcterms:description
"[A deeper understanding of the events arising as an early consequence of dystrophin deficiency in these two situations may strengthen approaches to therapy for DMD designed to improve muscle function and the quality of life.]. 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:18327663
;
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:NP154827.RA2jMqwiLZISIwURM5KLtJOnTp741bJLUz466QdZAWUJI130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:33:22+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" .
}