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> .
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> .
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http://www.w3.org/2001/XMLSchema#
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http://semanticscience.org/resource/
> .
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http://ncicb.nci.nih.gov/xml/owl/EVS/Thesaurus.owl#
> .
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http://linkedlifedata.com/resource/umls/id/
> .
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http://identifiers.org/ncbigene/
> .
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http://identifiers.org/pubmed/
> .
@prefix eco: <
http://purl.obolibrary.org/obo/
> .
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http://purl.org/ontology/wi/core#
> .
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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/v4.0.0/void/
> .
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{
this:
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np:Assertion
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ncit:C16612
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a
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.
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,
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dgn-np:NP729468.RAXL2RrILIHHjMpYmoYAkl1OXlcO9SDjWeri3roT5WW50130_assertion
dcterms:description
"[We report new clinical data supporting cosegregation of familial hemiplegic migraine and the new eye phenotype of elicited repetitive daily blindness and two novel SCN1A mutations as the underlying genetic defect in two unrelated families.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine."@en ;
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sio:SIO_000772
miriam-pubmed:19332696
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prov:wasGeneratedBy
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xsd:date
.
dgn-void:source_evidence_literature
a
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rdfs:comment
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rdfs:label
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dgn-np:NP729468.RAXL2RrILIHHjMpYmoYAkl1OXlcO9SDjWeri3roT5WW50130_publicationInfo
{
this:
dcterms:created
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xsd:dateTime
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dcterms:subject
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