@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP546434.RAEvhWrVV792XH-tqIObbn-WR5EWbDbGhkHbeLQp2EG-g
> .
@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:NP546434.RAEvhWrVV792XH-tqIObbn-WR5EWbDbGhkHbeLQp2EG-g130_head
{
this:
np:hasAssertion
dgn-np:NP546434.RAEvhWrVV792XH-tqIObbn-WR5EWbDbGhkHbeLQp2EG-g130_assertion
;
np:hasProvenance
dgn-np:NP546434.RAEvhWrVV792XH-tqIObbn-WR5EWbDbGhkHbeLQp2EG-g130_provenance
;
np:hasPublicationInfo
dgn-np:NP546434.RAEvhWrVV792XH-tqIObbn-WR5EWbDbGhkHbeLQp2EG-g130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP546434.RAEvhWrVV792XH-tqIObbn-WR5EWbDbGhkHbeLQp2EG-g130_assertion
a
np:Assertion
.
dgn-np:NP546434.RAEvhWrVV792XH-tqIObbn-WR5EWbDbGhkHbeLQp2EG-g130_provenance
a
np:Provenance
.
dgn-np:NP546434.RAEvhWrVV792XH-tqIObbn-WR5EWbDbGhkHbeLQp2EG-g130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP546434.RAEvhWrVV792XH-tqIObbn-WR5EWbDbGhkHbeLQp2EG-g130_assertion
{
miriam-gene:1807
a
ncit:C16612
.
lld:C0024591
a
ncit:C7057
.
dgn-gda:DGNf98e56e947e6edb5d1fc60062a3a37e7
sio:SIO_000628
miriam-gene:1807
,
lld:C0024591
;
a
sio:SIO_001121
.
}
dgn-np:NP546434.RAEvhWrVV792XH-tqIObbn-WR5EWbDbGhkHbeLQp2EG-g130_provenance
{
dgn-np:NP546434.RAEvhWrVV792XH-tqIObbn-WR5EWbDbGhkHbeLQp2EG-g130_assertion
dcterms:description
"[Our results exclude the alpha 1, beta 1, and gamma subunit of the DHP receptor as well as the SCN4A locus as candidates for the molecular defect in MHS for these pedigrees where also the RYR1 on chromosome 19q13.1 has been excluded.]. 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:8395939
;
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:NP546434.RAEvhWrVV792XH-tqIObbn-WR5EWbDbGhkHbeLQp2EG-g130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:37:29+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" .
}