@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP710865.RAYgpuEO2psuNbN1iW-s0kWCj18DLWjNxskVlkEYaJ5lQ
> .
@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:NP710865.RAYgpuEO2psuNbN1iW-s0kWCj18DLWjNxskVlkEYaJ5lQ130_head
{
this:
np:hasAssertion
dgn-np:NP710865.RAYgpuEO2psuNbN1iW-s0kWCj18DLWjNxskVlkEYaJ5lQ130_assertion
;
np:hasProvenance
dgn-np:NP710865.RAYgpuEO2psuNbN1iW-s0kWCj18DLWjNxskVlkEYaJ5lQ130_provenance
;
np:hasPublicationInfo
dgn-np:NP710865.RAYgpuEO2psuNbN1iW-s0kWCj18DLWjNxskVlkEYaJ5lQ130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP710865.RAYgpuEO2psuNbN1iW-s0kWCj18DLWjNxskVlkEYaJ5lQ130_assertion
a
np:Assertion
.
dgn-np:NP710865.RAYgpuEO2psuNbN1iW-s0kWCj18DLWjNxskVlkEYaJ5lQ130_provenance
a
np:Provenance
.
dgn-np:NP710865.RAYgpuEO2psuNbN1iW-s0kWCj18DLWjNxskVlkEYaJ5lQ130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP710865.RAYgpuEO2psuNbN1iW-s0kWCj18DLWjNxskVlkEYaJ5lQ130_assertion
{
miriam-gene:112476
a
ncit:C16612
.
lld:C0270862
a
ncit:C7057
.
dgn-gda:DGNbc6af53ba3b6f99704d0f8d869d06129
sio:SIO_000628
miriam-gene:112476
,
lld:C0270862
;
a
sio:SIO_001121
.
}
dgn-np:NP710865.RAYgpuEO2psuNbN1iW-s0kWCj18DLWjNxskVlkEYaJ5lQ130_provenance
{
dgn-np:NP710865.RAYgpuEO2psuNbN1iW-s0kWCj18DLWjNxskVlkEYaJ5lQ130_assertion
dcterms:description
"[The association of PKD and hemiplegic migraine has been previously reported in one large family, associated to febrile convulsions and afebrile seizures in some individuals, but our report relates this association of symptoms to a mutation in PRRT2.]. 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:23182655
;
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:NP710865.RAYgpuEO2psuNbN1iW-s0kWCj18DLWjNxskVlkEYaJ5lQ130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:39:12+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" .
}