@prefix this: <
http://rdf.disgenet.org/resource/nanopub/NP975533.RAicc5aXTie5Qg983KLJ6l-kU5FvV5LJH_IPzBe_MqdE4
> .
@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:NP975533.RAicc5aXTie5Qg983KLJ6l-kU5FvV5LJH_IPzBe_MqdE4130_head
{
this:
np:hasAssertion
dgn-np:NP975533.RAicc5aXTie5Qg983KLJ6l-kU5FvV5LJH_IPzBe_MqdE4130_assertion
;
np:hasProvenance
dgn-np:NP975533.RAicc5aXTie5Qg983KLJ6l-kU5FvV5LJH_IPzBe_MqdE4130_provenance
;
np:hasPublicationInfo
dgn-np:NP975533.RAicc5aXTie5Qg983KLJ6l-kU5FvV5LJH_IPzBe_MqdE4130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP975533.RAicc5aXTie5Qg983KLJ6l-kU5FvV5LJH_IPzBe_MqdE4130_assertion
a
np:Assertion
.
dgn-np:NP975533.RAicc5aXTie5Qg983KLJ6l-kU5FvV5LJH_IPzBe_MqdE4130_provenance
a
np:Provenance
.
dgn-np:NP975533.RAicc5aXTie5Qg983KLJ6l-kU5FvV5LJH_IPzBe_MqdE4130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP975533.RAicc5aXTie5Qg983KLJ6l-kU5FvV5LJH_IPzBe_MqdE4130_assertion
{
miriam-gene:149461
a
ncit:C16612
.
lld:C1279412
a
ncit:C7057
.
dgn-gda:DGN99a1a5bf5809af878032a4c9a1854995
sio:SIO_000628
miriam-gene:149461
,
lld:C1279412
;
a
sio:SIO_001121
.
}
dgn-np:NP975533.RAicc5aXTie5Qg983KLJ6l-kU5FvV5LJH_IPzBe_MqdE4130_provenance
{
dgn-np:NP975533.RAicc5aXTie5Qg983KLJ6l-kU5FvV5LJH_IPzBe_MqdE4130_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:NP975533.RAicc5aXTie5Qg983KLJ6l-kU5FvV5LJH_IPzBe_MqdE4130_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" .
}