@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP524284.RAexEStg7Exsz3vONj-yDd8IGgqdeQh3Bx0R2sLsiI4Js
> .
@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:NP524284.RAexEStg7Exsz3vONj-yDd8IGgqdeQh3Bx0R2sLsiI4Js130_head
{
this:
np:hasAssertion
dgn-np:NP524284.RAexEStg7Exsz3vONj-yDd8IGgqdeQh3Bx0R2sLsiI4Js130_assertion
;
np:hasProvenance
dgn-np:NP524284.RAexEStg7Exsz3vONj-yDd8IGgqdeQh3Bx0R2sLsiI4Js130_provenance
;
np:hasPublicationInfo
dgn-np:NP524284.RAexEStg7Exsz3vONj-yDd8IGgqdeQh3Bx0R2sLsiI4Js130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP524284.RAexEStg7Exsz3vONj-yDd8IGgqdeQh3Bx0R2sLsiI4Js130_assertion
a
np:Assertion
.
dgn-np:NP524284.RAexEStg7Exsz3vONj-yDd8IGgqdeQh3Bx0R2sLsiI4Js130_provenance
a
np:Provenance
.
dgn-np:NP524284.RAexEStg7Exsz3vONj-yDd8IGgqdeQh3Bx0R2sLsiI4Js130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP524284.RAexEStg7Exsz3vONj-yDd8IGgqdeQh3Bx0R2sLsiI4Js130_assertion
{
miriam-gene:9499
a
ncit:C16612
.
lld:C0026848
a
ncit:C7057
.
dgn-gda:DGN095a7e8cba9f01008a7268681ae417d8
sio:SIO_000628
miriam-gene:9499
,
lld:C0026848
;
a
sio:SIO_001121
.
}
dgn-np:NP524284.RAexEStg7Exsz3vONj-yDd8IGgqdeQh3Bx0R2sLsiI4Js130_provenance
{
dgn-np:NP524284.RAexEStg7Exsz3vONj-yDd8IGgqdeQh3Bx0R2sLsiI4Js130_assertion
dcterms:description
"[Understanding of this group of disorders has advanced in recent years through the identification of causative mutations in various genes, most of which encode proteins of the sarcomeric Z-disc, including desmin, alphaB-crystallin, myotilin, ZASP and filamin C. This review focuses on the MFMs arising from defects in these proteins, summarising genetic and clinical features of the disorders and then discussing emerging understanding of the molecular pathogenic mechanisms leading to muscle fibre degeneration.]. 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:18764962
;
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:NP524284.RAexEStg7Exsz3vONj-yDd8IGgqdeQh3Bx0R2sLsiI4Js130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:37:14+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" .
}