@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP591932.RAfTgyifInquZyK0TF1CmJZ0PnD4eeFUMpCL2tP-pXfK0
> .
@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:NP591932.RAfTgyifInquZyK0TF1CmJZ0PnD4eeFUMpCL2tP-pXfK0130_head
{
this:
np:hasAssertion
dgn-np:NP591932.RAfTgyifInquZyK0TF1CmJZ0PnD4eeFUMpCL2tP-pXfK0130_assertion
;
np:hasProvenance
dgn-np:NP591932.RAfTgyifInquZyK0TF1CmJZ0PnD4eeFUMpCL2tP-pXfK0130_provenance
;
np:hasPublicationInfo
dgn-np:NP591932.RAfTgyifInquZyK0TF1CmJZ0PnD4eeFUMpCL2tP-pXfK0130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP591932.RAfTgyifInquZyK0TF1CmJZ0PnD4eeFUMpCL2tP-pXfK0130_assertion
a
np:Assertion
.
dgn-np:NP591932.RAfTgyifInquZyK0TF1CmJZ0PnD4eeFUMpCL2tP-pXfK0130_provenance
a
np:Provenance
.
dgn-np:NP591932.RAfTgyifInquZyK0TF1CmJZ0PnD4eeFUMpCL2tP-pXfK0130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP591932.RAfTgyifInquZyK0TF1CmJZ0PnD4eeFUMpCL2tP-pXfK0130_assertion
{
miriam-gene:28988
a
ncit:C16612
.
lld:C0221055
a
ncit:C7057
.
dgn-gda:DGNf5c5708db548e9e22dccd5998a2177a3
sio:SIO_000628
miriam-gene:28988
,
lld:C0221055
;
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sio:SIO_001121
.
}
dgn-np:NP591932.RAfTgyifInquZyK0TF1CmJZ0PnD4eeFUMpCL2tP-pXfK0130_provenance
{
dgn-np:NP591932.RAfTgyifInquZyK0TF1CmJZ0PnD4eeFUMpCL2tP-pXfK0130_assertion
dcterms:description
"[Compound muscle action potential (CMAP) amplitudes, response to 2 Hz nerve stimulation, response to exercise and electromyographic needle electrode examination findings from the thenar muscles of two patients with paramyotonia congenita were compared with those from two patients with dominantly inherited myotonia congenita in warm (34 degrees C) and cold (20 degrees C) states.]. 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:6888415
;
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:NP591932.RAfTgyifInquZyK0TF1CmJZ0PnD4eeFUMpCL2tP-pXfK0130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:37:56+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
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dgn-void:disgenetrdf
pav:version
"v2.1.0" .
}