@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP499800.RAZJJc8nQamHvI-tPES9K_2-O7qIdI26Mw0lbfskFMcPg> .
@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:NP499800.RAZJJc8nQamHvI-tPES9K_2-O7qIdI26Mw0lbfskFMcPg130_head {
  this: np:hasAssertion dgn-np:NP499800.RAZJJc8nQamHvI-tPES9K_2-O7qIdI26Mw0lbfskFMcPg130_assertion ;
    np:hasProvenance dgn-np:NP499800.RAZJJc8nQamHvI-tPES9K_2-O7qIdI26Mw0lbfskFMcPg130_provenance ;
    np:hasPublicationInfo dgn-np:NP499800.RAZJJc8nQamHvI-tPES9K_2-O7qIdI26Mw0lbfskFMcPg130_publicationInfo ;
    a np:Nanopublication .
  dgn-np:NP499800.RAZJJc8nQamHvI-tPES9K_2-O7qIdI26Mw0lbfskFMcPg130_assertion a np:Assertion .
  dgn-np:NP499800.RAZJJc8nQamHvI-tPES9K_2-O7qIdI26Mw0lbfskFMcPg130_provenance a np:Provenance .
  dgn-np:NP499800.RAZJJc8nQamHvI-tPES9K_2-O7qIdI26Mw0lbfskFMcPg130_publicationInfo a np:PublicationInfo .
}
dgn-np:NP499800.RAZJJc8nQamHvI-tPES9K_2-O7qIdI26Mw0lbfskFMcPg130_assertion {
  miriam-gene:5972 a ncit:C16612 .
  lld:C0151786 a ncit:C7057 .
  dgn-gda:DGN74f01a4c3fa8cca53e417436bfba833e sio:SIO_000628 miriam-gene:5972 , lld:C0151786 ;
    a sio:SIO_001121 .
}
dgn-np:NP499800.RAZJJc8nQamHvI-tPES9K_2-O7qIdI26Mw0lbfskFMcPg130_provenance {
  dgn-np:NP499800.RAZJJc8nQamHvI-tPES9K_2-O7qIdI26Mw0lbfskFMcPg130_assertion dcterms:description "[These findings suggest a novel mechanism, involving the renin-angiotensin system, in the response of skeletal muscle to functional overload and may have implications for the management of conditions such as muscle wasting disorders, prolonged bed rest, ageing and rehabilitation, where muscle weakness may limit function.]. 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:11038409 ;
    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:NP499800.RAZJJc8nQamHvI-tPES9K_2-O7qIdI26Mw0lbfskFMcPg130_publicationInfo {
  this: dcterms:created "2014-10-02T12:36:58+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" .
}