@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP191794.RAtf5z5Inf8uACyLboLVjbKc-SiIklea6gjC38M_RHr0s
> .
@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:NP191794.RAtf5z5Inf8uACyLboLVjbKc-SiIklea6gjC38M_RHr0s130_head
{
this:
np:hasAssertion
dgn-np:NP191794.RAtf5z5Inf8uACyLboLVjbKc-SiIklea6gjC38M_RHr0s130_assertion
;
np:hasProvenance
dgn-np:NP191794.RAtf5z5Inf8uACyLboLVjbKc-SiIklea6gjC38M_RHr0s130_provenance
;
np:hasPublicationInfo
dgn-np:NP191794.RAtf5z5Inf8uACyLboLVjbKc-SiIklea6gjC38M_RHr0s130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP191794.RAtf5z5Inf8uACyLboLVjbKc-SiIklea6gjC38M_RHr0s130_assertion
a
np:Assertion
.
dgn-np:NP191794.RAtf5z5Inf8uACyLboLVjbKc-SiIklea6gjC38M_RHr0s130_provenance
a
np:Provenance
.
dgn-np:NP191794.RAtf5z5Inf8uACyLboLVjbKc-SiIklea6gjC38M_RHr0s130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP191794.RAtf5z5Inf8uACyLboLVjbKc-SiIklea6gjC38M_RHr0s130_assertion
{
miriam-gene:602
a
ncit:C16612
.
lld:C0024591
a
ncit:C7057
.
dgn-gda:DGNf34b2b8f00a649a242be2aa19f476c28
sio:SIO_000628
miriam-gene:602
,
lld:C0024591
;
a
sio:SIO_001121
.
}
dgn-np:NP191794.RAtf5z5Inf8uACyLboLVjbKc-SiIklea6gjC38M_RHr0s130_provenance
{
dgn-np:NP191794.RAtf5z5Inf8uACyLboLVjbKc-SiIklea6gjC38M_RHr0s130_assertion
dcterms:description
"[Molecular genetic linkage studies on the inherited human disorder malignant hyperthermia have resulted in the mapping of the locus for malignant hyperthermia susceptibility (MHS) to the twenty centimorgan genetic interval in the q12-13.2 region of chromosome 19 defined by the anonymous polymorphic DNA markers D19S9 and BCL3.]. 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:1973552
;
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:NP191794.RAtf5z5Inf8uACyLboLVjbKc-SiIklea6gjC38M_RHr0s130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:33:45+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" .
}