@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP811223.RA7k7JUfINeE_KegYL0xGqEWXi_x685Lrt_DKonepPt2A> .
@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:NP811223.RA7k7JUfINeE_KegYL0xGqEWXi_x685Lrt_DKonepPt2A130_head {
  this: np:hasAssertion dgn-np:NP811223.RA7k7JUfINeE_KegYL0xGqEWXi_x685Lrt_DKonepPt2A130_assertion ;
    np:hasProvenance dgn-np:NP811223.RA7k7JUfINeE_KegYL0xGqEWXi_x685Lrt_DKonepPt2A130_provenance ;
    np:hasPublicationInfo dgn-np:NP811223.RA7k7JUfINeE_KegYL0xGqEWXi_x685Lrt_DKonepPt2A130_publicationInfo ;
    a np:Nanopublication .
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}
dgn-np:NP811223.RA7k7JUfINeE_KegYL0xGqEWXi_x685Lrt_DKonepPt2A130_assertion {
  miriam-gene:7273 a ncit:C16612 .
  lld:C0018817 a ncit:C7057 .
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    a sio:SIO_001121 .
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dgn-np:NP811223.RA7k7JUfINeE_KegYL0xGqEWXi_x685Lrt_DKonepPt2A130_provenance {
  dgn-np:NP811223.RA7k7JUfINeE_KegYL0xGqEWXi_x685Lrt_DKonepPt2A130_assertion dcterms:description "[To assess the role of sarcomeric genes in patients with inherited ASDII, we analyzed 13 sarcomeric genes (MYH7, MYBPC3, TNNT2, TCAP, TNNI3, MYH6, TPM1, MYL2, CSRP3, ACTC1, MYL3, TNNC1, and TTN kinase region) in 31 patients with familial ASDII using array-based resequencing.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine."@en ;
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    rdfs:comment "Gene-disease associations inferred from text-mining the literature."@en ;
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dgn-np:NP811223.RA7k7JUfINeE_KegYL0xGqEWXi_x685Lrt_DKonepPt2A130_publicationInfo {
  this: dcterms:created "2014-10-02T12:40:17+02:00"^^xsd:dateTime ;
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    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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