@prefix this: <
http://rdf.disgenet.org/resource/nanopub/NP477527.RAE4cFTQjqqDxMcD4x_AAzVjq6iTGLqnk1l4-G_m66Vtw
> .
@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/
> .
@prefix wi: <
http://purl.org/ontology/wi/core#
> .
@prefix prov: <
http://www.w3.org/ns/prov#
> .
@prefix pav: <
http://purl.org/pav/
> .
@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/resource/nanopub/
> .
@prefix dgn-gda: <
http://rdf.disgenet.org/resource/gda/
> .
@prefix dgn-void: <
http://rdf.disgenet.org/v4.0.0/void/
> .
dgn-np:NP477527.RAE4cFTQjqqDxMcD4x_AAzVjq6iTGLqnk1l4-G_m66Vtw130_head
{
this:
np:hasAssertion
dgn-np:NP477527.RAE4cFTQjqqDxMcD4x_AAzVjq6iTGLqnk1l4-G_m66Vtw130_assertion
;
np:hasProvenance
dgn-np:NP477527.RAE4cFTQjqqDxMcD4x_AAzVjq6iTGLqnk1l4-G_m66Vtw130_provenance
;
np:hasPublicationInfo
dgn-np:NP477527.RAE4cFTQjqqDxMcD4x_AAzVjq6iTGLqnk1l4-G_m66Vtw130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP477527.RAE4cFTQjqqDxMcD4x_AAzVjq6iTGLqnk1l4-G_m66Vtw130_assertion
a
np:Assertion
.
dgn-np:NP477527.RAE4cFTQjqqDxMcD4x_AAzVjq6iTGLqnk1l4-G_m66Vtw130_provenance
a
np:Provenance
.
dgn-np:NP477527.RAE4cFTQjqqDxMcD4x_AAzVjq6iTGLqnk1l4-G_m66Vtw130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP477527.RAE4cFTQjqqDxMcD4x_AAzVjq6iTGLqnk1l4-G_m66Vtw130_assertion
{
miriam-gene:1756
a
ncit:C16612
.
lld:C0026850
a
ncit:C7057
.
dgn-gda:DGN619f314925fa6c68de6fe3061aac7cbe
sio:SIO_000628
miriam-gene:1756
,
lld:C0026850
;
a
sio:SIO_001121
.
}
dgn-np:NP477527.RAE4cFTQjqqDxMcD4x_AAzVjq6iTGLqnk1l4-G_m66Vtw130_provenance
{
dgn-np:NP477527.RAE4cFTQjqqDxMcD4x_AAzVjq6iTGLqnk1l4-G_m66Vtw130_assertion
dcterms:description
"[Life-time monitoring of the main clinical and laboratory manifestations of hereditary muscular dystrophy in mdx mice confirmed the presence of mutation in exon 23 of dystrophin gene and the absence of this protein in skeletal muscles of mutant animals.]. 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:15665963
;
prov:wasDerivedFrom
dgn-void:befree-2016
;
prov:wasGeneratedBy
eco:ECO_0000203
.
dgn-void:befree-2016
pav:importedOn
"2016-02-19"^^
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:NP477527.RAE4cFTQjqqDxMcD4x_AAzVjq6iTGLqnk1l4-G_m66Vtw130_publicationInfo
{
this:
dcterms:created
"2016-05-13T12:45:21+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:disgenetv3.0rdf
;
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
"v4.0.0.0" .
dgn-void:disgenetv3.0rdf
pav:version
"v4.0.0" .
}