@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP765580.RATdzcnfEPFjKFTT_Ye8TuVf7CyYRUHrEDc7R_e8NKkpI> .
@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:NP765580.RATdzcnfEPFjKFTT_Ye8TuVf7CyYRUHrEDc7R_e8NKkpI130_head {
  this: np:hasAssertion dgn-np:NP765580.RATdzcnfEPFjKFTT_Ye8TuVf7CyYRUHrEDc7R_e8NKkpI130_assertion;
    np:hasProvenance dgn-np:NP765580.RATdzcnfEPFjKFTT_Ye8TuVf7CyYRUHrEDc7R_e8NKkpI130_provenance;
    np:hasPublicationInfo dgn-np:NP765580.RATdzcnfEPFjKFTT_Ye8TuVf7CyYRUHrEDc7R_e8NKkpI130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP765580.RATdzcnfEPFjKFTT_Ye8TuVf7CyYRUHrEDc7R_e8NKkpI130_assertion a np:Assertion .
  
  dgn-np:NP765580.RATdzcnfEPFjKFTT_Ye8TuVf7CyYRUHrEDc7R_e8NKkpI130_provenance a np:Provenance .
  
  dgn-np:NP765580.RATdzcnfEPFjKFTT_Ye8TuVf7CyYRUHrEDc7R_e8NKkpI130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP765580.RATdzcnfEPFjKFTT_Ye8TuVf7CyYRUHrEDc7R_e8NKkpI130_assertion {
  miriam-gene:55795 a ncit:C16612 .
  
  lld:C0026837 a ncit:C7057 .
  
  dgn-gda:DGNc28ffa25d89dc4246ded80669bc3361d sio:SIO_000628 miriam-gene:55795, lld:C0026837;
    a sio:SIO_001121 .
}

dgn-np:NP765580.RATdzcnfEPFjKFTT_Ye8TuVf7CyYRUHrEDc7R_e8NKkpI130_provenance {
  dgn-np:NP765580.RATdzcnfEPFjKFTT_Ye8TuVf7CyYRUHrEDc7R_e8NKkpI130_assertion dcterms:description
      "[Major findings of this study for mutation R723G were i), a >40% increase in fiber stiffness in rigor with a 2.9-fold increase in stiffness per myosin head (S( *)(rigor R723G) = 0.84 pN/nm S( *)(rigor WT) = 0.29 pN/nm); and ii), a significant increase in force per head (F( *)(10 degrees C), 1.99 pN vs. 1.49 pN = 1.3-fold increase; F( *)(20 degrees C), 2.56 pN vs. 1.92 pN = 1.3-fold increase) as well as stiffness per head during isometric steady-state contraction (S( *)(active10 degrees C), 0.52 pN/nm vs. 0.28 pN/nm = 1.9-fold increase).]. 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:19651039;
    prov:wasDerivedFrom dgn-void:befree-20140225;
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  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:NP765580.RATdzcnfEPFjKFTT_Ye8TuVf7CyYRUHrEDc7R_e8NKkpI130_publicationInfo {
  this: dcterms:created "2014-10-02T12:39:43+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>,
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    pav:version "v2.1.0.0" .
  
  dgn-void:disgenetrdf pav:version "v2.1.0" .
}