Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP514178.RAJfF6NBFnjwTqqqu188XdrBWvNx5XIR2T7EWCWlusQd0130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP514178.RAJfF6NBFnjwTqqqu188XdrBWvNx5XIR2T7EWCWlusQd0130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP514178.RAJfF6NBFnjwTqqqu188XdrBWvNx5XIR2T7EWCWlusQd0130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP514178.RAJfF6NBFnjwTqqqu188XdrBWvNx5XIR2T7EWCWlusQd0130_provenance.
- NP514178.RAJfF6NBFnjwTqqqu188XdrBWvNx5XIR2T7EWCWlusQd0130_assertion description "[MYH9-related disease ( MYH9-RD) is an autosomal dominant thrombocytopenia with giant platelets variably associated with young-adult onset of progressive sensorineural hearing loss, presenile cataract, and renal damage.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP514178.RAJfF6NBFnjwTqqqu188XdrBWvNx5XIR2T7EWCWlusQd0130_provenance.
- NP514178.RAJfF6NBFnjwTqqqu188XdrBWvNx5XIR2T7EWCWlusQd0130_assertion evidence source_evidence_literature NP514178.RAJfF6NBFnjwTqqqu188XdrBWvNx5XIR2T7EWCWlusQd0130_provenance.
- NP514178.RAJfF6NBFnjwTqqqu188XdrBWvNx5XIR2T7EWCWlusQd0130_assertion SIO_000772 20174760 NP514178.RAJfF6NBFnjwTqqqu188XdrBWvNx5XIR2T7EWCWlusQd0130_provenance.
- NP514178.RAJfF6NBFnjwTqqqu188XdrBWvNx5XIR2T7EWCWlusQd0130_assertion wasDerivedFrom befree-20140225 NP514178.RAJfF6NBFnjwTqqqu188XdrBWvNx5XIR2T7EWCWlusQd0130_provenance.
- NP514178.RAJfF6NBFnjwTqqqu188XdrBWvNx5XIR2T7EWCWlusQd0130_assertion wasGeneratedBy ECO_0000203 NP514178.RAJfF6NBFnjwTqqqu188XdrBWvNx5XIR2T7EWCWlusQd0130_provenance.
- befree-20140225 importedOn "2014-02-25" NP514178.RAJfF6NBFnjwTqqqu188XdrBWvNx5XIR2T7EWCWlusQd0130_provenance.