@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP738295.RAN7ZYIig4kU7CfDe5Ar21XMjJHt78LFJlINBgR2Ky2Mg
> .
@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:NP738295.RAN7ZYIig4kU7CfDe5Ar21XMjJHt78LFJlINBgR2Ky2Mg130_head
{
this:
np:hasAssertion
dgn-np:NP738295.RAN7ZYIig4kU7CfDe5Ar21XMjJHt78LFJlINBgR2Ky2Mg130_assertion
;
np:hasProvenance
dgn-np:NP738295.RAN7ZYIig4kU7CfDe5Ar21XMjJHt78LFJlINBgR2Ky2Mg130_provenance
;
np:hasPublicationInfo
dgn-np:NP738295.RAN7ZYIig4kU7CfDe5Ar21XMjJHt78LFJlINBgR2Ky2Mg130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP738295.RAN7ZYIig4kU7CfDe5Ar21XMjJHt78LFJlINBgR2Ky2Mg130_assertion
a
np:Assertion
.
dgn-np:NP738295.RAN7ZYIig4kU7CfDe5Ar21XMjJHt78LFJlINBgR2Ky2Mg130_provenance
a
np:Provenance
.
dgn-np:NP738295.RAN7ZYIig4kU7CfDe5Ar21XMjJHt78LFJlINBgR2Ky2Mg130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP738295.RAN7ZYIig4kU7CfDe5Ar21XMjJHt78LFJlINBgR2Ky2Mg130_assertion
{
miriam-gene:6261
a
ncit:C16612
.
lld:C0151786
a
ncit:C7057
.
dgn-gda:DGNcb83f77ddb4cdacee485690e6643e3a4
sio:SIO_000628
miriam-gene:6261
,
lld:C0151786
;
a
sio:SIO_001121
.
}
dgn-np:NP738295.RAN7ZYIig4kU7CfDe5Ar21XMjJHt78LFJlINBgR2Ky2Mg130_provenance
{
dgn-np:NP738295.RAN7ZYIig4kU7CfDe5Ar21XMjJHt78LFJlINBgR2Ky2Mg130_assertion
dcterms:description
"[Two fundamentally distinct cellular mechanisms (leaky channels and EC uncoupling) are proposed to explain how altered release channel function caused by different mutations in RyR1 could result in muscle weakness in CCD.]. 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:11524458
;
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:NP738295.RAN7ZYIig4kU7CfDe5Ar21XMjJHt78LFJlINBgR2Ky2Mg130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:39:28+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" .
}