@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP494202.RA5IEPlHGeeYl1mhNaQTnkmbYZ15s1AMHgGcOltlY4zKs
> .
@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:NP494202.RA5IEPlHGeeYl1mhNaQTnkmbYZ15s1AMHgGcOltlY4zKs130_head
{
this:
np:hasAssertion
dgn-np:NP494202.RA5IEPlHGeeYl1mhNaQTnkmbYZ15s1AMHgGcOltlY4zKs130_assertion
;
np:hasProvenance
dgn-np:NP494202.RA5IEPlHGeeYl1mhNaQTnkmbYZ15s1AMHgGcOltlY4zKs130_provenance
;
np:hasPublicationInfo
dgn-np:NP494202.RA5IEPlHGeeYl1mhNaQTnkmbYZ15s1AMHgGcOltlY4zKs130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP494202.RA5IEPlHGeeYl1mhNaQTnkmbYZ15s1AMHgGcOltlY4zKs130_assertion
a
np:Assertion
.
dgn-np:NP494202.RA5IEPlHGeeYl1mhNaQTnkmbYZ15s1AMHgGcOltlY4zKs130_provenance
a
np:Provenance
.
dgn-np:NP494202.RA5IEPlHGeeYl1mhNaQTnkmbYZ15s1AMHgGcOltlY4zKs130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP494202.RA5IEPlHGeeYl1mhNaQTnkmbYZ15s1AMHgGcOltlY4zKs130_assertion
{
miriam-gene:203859
a
ncit:C16612
.
lld:C0026850
a
ncit:C7057
.
dgn-gda:DGNed2a3cc3663ae3770bfd957db40499ab
sio:SIO_000628
miriam-gene:203859
,
lld:C0026850
;
a
sio:SIO_001121
.
}
dgn-np:NP494202.RA5IEPlHGeeYl1mhNaQTnkmbYZ15s1AMHgGcOltlY4zKs130_provenance
{
dgn-np:NP494202.RA5IEPlHGeeYl1mhNaQTnkmbYZ15s1AMHgGcOltlY4zKs130_assertion
dcterms:description
"[The cases reported here should help to better understand the important role of mutation screening in the ANO5 gene in patients with adult onset muscular dystrophy and very high CK levels.]. 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:22499103
;
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:NP494202.RA5IEPlHGeeYl1mhNaQTnkmbYZ15s1AMHgGcOltlY4zKs130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:36:55+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
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"v2.1.0" .
}