@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP562491.RAlPtNQWaP_F2NGTA--QHYVEdzLYLjJUNn6o2X0H_rs3Q> .
@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:NP562491.RAlPtNQWaP_F2NGTA--QHYVEdzLYLjJUNn6o2X0H_rs3Q130_head {
   this: np:hasAssertion dgn-np:NP562491.RAlPtNQWaP_F2NGTA--QHYVEdzLYLjJUNn6o2X0H_rs3Q130_assertion ;
    np:hasProvenance dgn-np:NP562491.RAlPtNQWaP_F2NGTA--QHYVEdzLYLjJUNn6o2X0H_rs3Q130_provenance ;
    np:hasPublicationInfo dgn-np:NP562491.RAlPtNQWaP_F2NGTA--QHYVEdzLYLjJUNn6o2X0H_rs3Q130_publicationInfo ;
    a np:Nanopublication .
  dgn-np:NP562491.RAlPtNQWaP_F2NGTA--QHYVEdzLYLjJUNn6o2X0H_rs3Q130_assertion a np:Assertion .
  dgn-np:NP562491.RAlPtNQWaP_F2NGTA--QHYVEdzLYLjJUNn6o2X0H_rs3Q130_provenance a np:Provenance .
  dgn-np:NP562491.RAlPtNQWaP_F2NGTA--QHYVEdzLYLjJUNn6o2X0H_rs3Q130_publicationInfo a np:PublicationInfo .
}
dgn-np:NP562491.RAlPtNQWaP_F2NGTA--QHYVEdzLYLjJUNn6o2X0H_rs3Q130_assertion {
   miriam-gene:477 a ncit:C16612 .
  lld:C1832903 a ncit:C7057 .
  dgn-gda:DGNf2a6125be525ffd00869567b9fbdea02 sio:SIO_000628 miriam-gene:477 , lld:C1832903 ;
    a sio:SIO_001121 .
}
dgn-np:NP562491.RAlPtNQWaP_F2NGTA--QHYVEdzLYLjJUNn6o2X0H_rs3Q130_provenance {
   dgn-np:NP562491.RAlPtNQWaP_F2NGTA--QHYVEdzLYLjJUNn6o2X0H_rs3Q130_assertion dcterms:description "[In this study, we examined the functional properties of 11 ATP1A2 mutations associated with familial or sporadic hemiplegic migraine, including missense mutations (T263M, T376M, R383H, A606T, R763H, M829R, R834Q, R937P, and X1021R), a deletion mutant (del(K935-S940)ins(I)), and a frameshift mutation (S966fs).]. 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:18728015 ;
    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:NP562491.RAlPtNQWaP_F2NGTA--QHYVEdzLYLjJUNn6o2X0H_rs3Q130_publicationInfo {
   this: dcterms:created "2014-10-02T12:37:39+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> ;
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}