Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP317806.RAFfW-U6R9kIHG9rHhwznZW_HvZ2iAxGheUpamsmzKUjc130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP317806.RAFfW-U6R9kIHG9rHhwznZW_HvZ2iAxGheUpamsmzKUjc130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP317806.RAFfW-U6R9kIHG9rHhwznZW_HvZ2iAxGheUpamsmzKUjc130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP317806.RAFfW-U6R9kIHG9rHhwznZW_HvZ2iAxGheUpamsmzKUjc130_provenance.
- NP317806.RAFfW-U6R9kIHG9rHhwznZW_HvZ2iAxGheUpamsmzKUjc130_assertion description "[Complete loss of expression of the ANT1 gene causing cardiomyopathy and myopathy.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP317806.RAFfW-U6R9kIHG9rHhwznZW_HvZ2iAxGheUpamsmzKUjc130_provenance.
- NP317806.RAFfW-U6R9kIHG9rHhwznZW_HvZ2iAxGheUpamsmzKUjc130_assertion evidence source_evidence_literature NP317806.RAFfW-U6R9kIHG9rHhwznZW_HvZ2iAxGheUpamsmzKUjc130_provenance.
- NP317806.RAFfW-U6R9kIHG9rHhwznZW_HvZ2iAxGheUpamsmzKUjc130_assertion SIO_000772 22187496 NP317806.RAFfW-U6R9kIHG9rHhwznZW_HvZ2iAxGheUpamsmzKUjc130_provenance.
- NP317806.RAFfW-U6R9kIHG9rHhwznZW_HvZ2iAxGheUpamsmzKUjc130_assertion wasDerivedFrom befree-20140225 NP317806.RAFfW-U6R9kIHG9rHhwznZW_HvZ2iAxGheUpamsmzKUjc130_provenance.
- NP317806.RAFfW-U6R9kIHG9rHhwznZW_HvZ2iAxGheUpamsmzKUjc130_assertion wasGeneratedBy ECO_0000203 NP317806.RAFfW-U6R9kIHG9rHhwznZW_HvZ2iAxGheUpamsmzKUjc130_provenance.
- befree-20140225 importedOn "2014-02-25" NP317806.RAFfW-U6R9kIHG9rHhwznZW_HvZ2iAxGheUpamsmzKUjc130_provenance.