@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP369672.RAwfDEdK46KvdPbSTGMoRVGbRyKOKFVJn89KgOI08YEFQ
> .
@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:NP369672.RAwfDEdK46KvdPbSTGMoRVGbRyKOKFVJn89KgOI08YEFQ130_head
{
this:
np:hasAssertion
dgn-np:NP369672.RAwfDEdK46KvdPbSTGMoRVGbRyKOKFVJn89KgOI08YEFQ130_assertion
;
np:hasProvenance
dgn-np:NP369672.RAwfDEdK46KvdPbSTGMoRVGbRyKOKFVJn89KgOI08YEFQ130_provenance
;
np:hasPublicationInfo
dgn-np:NP369672.RAwfDEdK46KvdPbSTGMoRVGbRyKOKFVJn89KgOI08YEFQ130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP369672.RAwfDEdK46KvdPbSTGMoRVGbRyKOKFVJn89KgOI08YEFQ130_assertion
a
np:Assertion
.
dgn-np:NP369672.RAwfDEdK46KvdPbSTGMoRVGbRyKOKFVJn89KgOI08YEFQ130_provenance
a
np:Provenance
.
dgn-np:NP369672.RAwfDEdK46KvdPbSTGMoRVGbRyKOKFVJn89KgOI08YEFQ130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP369672.RAwfDEdK46KvdPbSTGMoRVGbRyKOKFVJn89KgOI08YEFQ130_assertion
{
miriam-gene:7439
a
ncit:C16612
.
lld:C0026850
a
ncit:C7057
.
dgn-gda:DGN37a70cffa67668c39b0b8468832abff6
sio:SIO_000628
miriam-gene:7439
,
lld:C0026850
;
a
sio:SIO_001121
.
}
dgn-np:NP369672.RAwfDEdK46KvdPbSTGMoRVGbRyKOKFVJn89KgOI08YEFQ130_provenance
{
dgn-np:NP369672.RAwfDEdK46KvdPbSTGMoRVGbRyKOKFVJn89KgOI08YEFQ130_assertion
dcterms:description
"[The discovery of the dystrophin gene, whose mutations lead to Duchenne's and Becker's muscular dystrophy (DMD and BMD), represents the first important landmark by which, in the last ten years, molecular biology and genetic studies have revealed many of the molecular defects of the major muscular dystrophies.]. 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:10937856
;
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:NP369672.RAwfDEdK46KvdPbSTGMoRVGbRyKOKFVJn89KgOI08YEFQ130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:35:36+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" .
}