Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP948338.RAXlMkZQ1rcXSyI4jTXR52pYurKLphuN95VhcguLEFVnU130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP948338.RAXlMkZQ1rcXSyI4jTXR52pYurKLphuN95VhcguLEFVnU130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP948338.RAXlMkZQ1rcXSyI4jTXR52pYurKLphuN95VhcguLEFVnU130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP948338.RAXlMkZQ1rcXSyI4jTXR52pYurKLphuN95VhcguLEFVnU130_provenance.
- NP948338.RAXlMkZQ1rcXSyI4jTXR52pYurKLphuN95VhcguLEFVnU130_assertion description "[This report expands the clinical spectrum of ANT1-related human diseases, and emphasises the crucial role of the mitochondrial ADP/ATP carriers in muscle function and pathophysiology of human myopathies.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP948338.RAXlMkZQ1rcXSyI4jTXR52pYurKLphuN95VhcguLEFVnU130_provenance.
- NP948338.RAXlMkZQ1rcXSyI4jTXR52pYurKLphuN95VhcguLEFVnU130_assertion evidence source_evidence_literature NP948338.RAXlMkZQ1rcXSyI4jTXR52pYurKLphuN95VhcguLEFVnU130_provenance.
- NP948338.RAXlMkZQ1rcXSyI4jTXR52pYurKLphuN95VhcguLEFVnU130_assertion SIO_000772 22187496 NP948338.RAXlMkZQ1rcXSyI4jTXR52pYurKLphuN95VhcguLEFVnU130_provenance.
- NP948338.RAXlMkZQ1rcXSyI4jTXR52pYurKLphuN95VhcguLEFVnU130_assertion wasDerivedFrom befree-2016 NP948338.RAXlMkZQ1rcXSyI4jTXR52pYurKLphuN95VhcguLEFVnU130_provenance.
- NP948338.RAXlMkZQ1rcXSyI4jTXR52pYurKLphuN95VhcguLEFVnU130_assertion wasGeneratedBy ECO_0000203 NP948338.RAXlMkZQ1rcXSyI4jTXR52pYurKLphuN95VhcguLEFVnU130_provenance.
- befree-2016 importedOn "2016-02-19" NP948338.RAXlMkZQ1rcXSyI4jTXR52pYurKLphuN95VhcguLEFVnU130_provenance.