@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP163762.RAHm69AtQ1xHipCLSrBWAm2QtlDZJs3wFOC21XwFCUijU
> .
@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:NP163762.RAHm69AtQ1xHipCLSrBWAm2QtlDZJs3wFOC21XwFCUijU130_head
{
this:
np:hasAssertion
dgn-np:NP163762.RAHm69AtQ1xHipCLSrBWAm2QtlDZJs3wFOC21XwFCUijU130_assertion
;
np:hasProvenance
dgn-np:NP163762.RAHm69AtQ1xHipCLSrBWAm2QtlDZJs3wFOC21XwFCUijU130_provenance
;
np:hasPublicationInfo
dgn-np:NP163762.RAHm69AtQ1xHipCLSrBWAm2QtlDZJs3wFOC21XwFCUijU130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP163762.RAHm69AtQ1xHipCLSrBWAm2QtlDZJs3wFOC21XwFCUijU130_assertion
a
np:Assertion
.
dgn-np:NP163762.RAHm69AtQ1xHipCLSrBWAm2QtlDZJs3wFOC21XwFCUijU130_provenance
a
np:Provenance
.
dgn-np:NP163762.RAHm69AtQ1xHipCLSrBWAm2QtlDZJs3wFOC21XwFCUijU130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP163762.RAHm69AtQ1xHipCLSrBWAm2QtlDZJs3wFOC21XwFCUijU130_assertion
{
miriam-gene:1756
a
ncit:C16612
.
lld:C0917713
a
ncit:C7057
.
dgn-gda:DGNe4fd5f0178adfed1dba03dd72f78980a
sio:SIO_000628
miriam-gene:1756
,
lld:C0917713
;
a
sio:SIO_001121
.
}
dgn-np:NP163762.RAHm69AtQ1xHipCLSrBWAm2QtlDZJs3wFOC21XwFCUijU130_provenance
{
dgn-np:NP163762.RAHm69AtQ1xHipCLSrBWAm2QtlDZJs3wFOC21XwFCUijU130_assertion
dcterms:description
"[Duchenne and Becker muscular dystrophy (DMD and BMD, respectively) are allelic disorders with different clinical presentations and severity determined by mutations in the gene DMD, which encodes the sarcolemmal protein dystrophin.]. 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:21399986
;
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:NP163762.RAHm69AtQ1xHipCLSrBWAm2QtlDZJs3wFOC21XwFCUijU130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:33:28+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" .
}