@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP529922.RAs3UH7i_P7QAdXlbBKb7UEPsA3Xspr152maRNs0CzVN0
> .
@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:NP529922.RAs3UH7i_P7QAdXlbBKb7UEPsA3Xspr152maRNs0CzVN0130_head
{
this:
np:hasAssertion
dgn-np:NP529922.RAs3UH7i_P7QAdXlbBKb7UEPsA3Xspr152maRNs0CzVN0130_assertion
;
np:hasProvenance
dgn-np:NP529922.RAs3UH7i_P7QAdXlbBKb7UEPsA3Xspr152maRNs0CzVN0130_provenance
;
np:hasPublicationInfo
dgn-np:NP529922.RAs3UH7i_P7QAdXlbBKb7UEPsA3Xspr152maRNs0CzVN0130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP529922.RAs3UH7i_P7QAdXlbBKb7UEPsA3Xspr152maRNs0CzVN0130_assertion
a
np:Assertion
.
dgn-np:NP529922.RAs3UH7i_P7QAdXlbBKb7UEPsA3Xspr152maRNs0CzVN0130_provenance
a
np:Provenance
.
dgn-np:NP529922.RAs3UH7i_P7QAdXlbBKb7UEPsA3Xspr152maRNs0CzVN0130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP529922.RAs3UH7i_P7QAdXlbBKb7UEPsA3Xspr152maRNs0CzVN0130_assertion
{
miriam-gene:1756
a
ncit:C16612
.
lld:C0086525
a
ncit:C7057
.
dgn-gda:DGN3e055f12ee6e40d021d487423b47fc00
sio:SIO_000628
miriam-gene:1756
,
lld:C0086525
;
a
sio:SIO_001121
.
}
dgn-np:NP529922.RAs3UH7i_P7QAdXlbBKb7UEPsA3Xspr152maRNs0CzVN0130_provenance
{
dgn-np:NP529922.RAs3UH7i_P7QAdXlbBKb7UEPsA3Xspr152maRNs0CzVN0130_assertion
dcterms:description
"[Whereas the specific mechanisms leading to muscle pathology in Duchenne muscular dystrophy are still being debated it is apparent that the progressive weakness that occurs in this disease is the result of a chronic process that is initiated by dystrophin deficiency.]. 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:1821686
;
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:NP529922.RAs3UH7i_P7QAdXlbBKb7UEPsA3Xspr152maRNs0CzVN0130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:37:20+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" .
}