@prefix this: <
http://rdf.disgenet.org/resource/nanopub/NP869969.RAZtfyVOzQpvwKkSTP7LTWPOQFVYW3yR7GjNl2y1hhEr4
> .
@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:NP869969.RAZtfyVOzQpvwKkSTP7LTWPOQFVYW3yR7GjNl2y1hhEr4130_head
{
this:
np:hasAssertion
dgn-np:NP869969.RAZtfyVOzQpvwKkSTP7LTWPOQFVYW3yR7GjNl2y1hhEr4130_assertion
;
np:hasProvenance
dgn-np:NP869969.RAZtfyVOzQpvwKkSTP7LTWPOQFVYW3yR7GjNl2y1hhEr4130_provenance
;
np:hasPublicationInfo
dgn-np:NP869969.RAZtfyVOzQpvwKkSTP7LTWPOQFVYW3yR7GjNl2y1hhEr4130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP869969.RAZtfyVOzQpvwKkSTP7LTWPOQFVYW3yR7GjNl2y1hhEr4130_assertion
a
np:Assertion
.
dgn-np:NP869969.RAZtfyVOzQpvwKkSTP7LTWPOQFVYW3yR7GjNl2y1hhEr4130_provenance
a
np:Provenance
.
dgn-np:NP869969.RAZtfyVOzQpvwKkSTP7LTWPOQFVYW3yR7GjNl2y1hhEr4130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP869969.RAZtfyVOzQpvwKkSTP7LTWPOQFVYW3yR7GjNl2y1hhEr4130_assertion
{
miriam-gene:6261
a
ncit:C16612
.
lld:C0026848
a
ncit:C7057
.
dgn-gda:DGN735258e8984fadee8cf3ced0600f6d13
sio:SIO_000628
miriam-gene:6261
,
lld:C0026848
;
a
sio:SIO_001121
.
}
dgn-np:NP869969.RAZtfyVOzQpvwKkSTP7LTWPOQFVYW3yR7GjNl2y1hhEr4130_provenance
{
dgn-np:NP869969.RAZtfyVOzQpvwKkSTP7LTWPOQFVYW3yR7GjNl2y1hhEr4130_assertion
dcterms:description
"[In this review, we discuss the mutations that cause skeletal myopathies and cardiac arrhythmias and how these mutations pinpoint residues within the RyR protein that are functionally significant and might be developed as targets for therapeutic drugs.]. 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:21291389
;
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:NP869969.RAZtfyVOzQpvwKkSTP7LTWPOQFVYW3yR7GjNl2y1hhEr4130_publicationInfo
{
this:
dcterms:created
"2016-05-13T12:48:19+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" .
}