@prefix this: <
http://rdf.disgenet.org/resource/nanopub/NP975532.RApXwmcedRDM_R9Jhl9wNhF5IDhjum7S_Xye2-U2K9ZP0
> .
@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/v3.0.0/void/
> .
dgn-np:NP975532.RApXwmcedRDM_R9Jhl9wNhF5IDhjum7S_Xye2-U2K9ZP0130_head
{
this:
np:hasAssertion
dgn-np:NP975532.RApXwmcedRDM_R9Jhl9wNhF5IDhjum7S_Xye2-U2K9ZP0130_assertion
;
np:hasProvenance
dgn-np:NP975532.RApXwmcedRDM_R9Jhl9wNhF5IDhjum7S_Xye2-U2K9ZP0130_provenance
;
np:hasPublicationInfo
dgn-np:NP975532.RApXwmcedRDM_R9Jhl9wNhF5IDhjum7S_Xye2-U2K9ZP0130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP975532.RApXwmcedRDM_R9Jhl9wNhF5IDhjum7S_Xye2-U2K9ZP0130_assertion
a
np:Assertion
.
dgn-np:NP975532.RApXwmcedRDM_R9Jhl9wNhF5IDhjum7S_Xye2-U2K9ZP0130_provenance
a
np:Provenance
.
dgn-np:NP975532.RApXwmcedRDM_R9Jhl9wNhF5IDhjum7S_Xye2-U2K9ZP0130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP975532.RApXwmcedRDM_R9Jhl9wNhF5IDhjum7S_Xye2-U2K9ZP0130_assertion
{
miriam-gene:149461
a
ncit:C16612
.
lld:C0424551
a
ncit:C7057
.
dgn-gda:DGN36f5e19970ddfe47055d3921d2a12835
sio:SIO_000628
miriam-gene:149461
,
lld:C0424551
;
a
sio:SIO_001121
.
}
dgn-np:NP975532.RApXwmcedRDM_R9Jhl9wNhF5IDhjum7S_Xye2-U2K9ZP0130_provenance
{
dgn-np:NP975532.RApXwmcedRDM_R9Jhl9wNhF5IDhjum7S_Xye2-U2K9ZP0130_assertion
dcterms:description
"[Ocular manifestations, even subtle, and exercise intolerance mimicking mild to moderate periodic paralysis are two symptoms that need to be searched for in patients with FHHNC and may indicate CLDN19 mutations.]. 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:21030577
;
prov:wasDerivedFrom
dgn-void:befree-20150227
;
prov:wasGeneratedBy
eco:ECO_0000203
.
dgn-void:befree-20150227
pav:importedOn
"2015-02-27"^^
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:NP975532.RApXwmcedRDM_R9Jhl9wNhF5IDhjum7S_Xye2-U2K9ZP0130_publicationInfo
{
this:
dcterms:created
"2015-08-25T14:47:36+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
"v3.0.0.0" .
dgn-void:disgenetv3.0rdf
pav:version
"v3.0.0" .
}