Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP676057.RAe9oSvz-MXgtoSinW_W1aAcmavd7c0fkrwgmB9aDW6sc130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP676057.RAe9oSvz-MXgtoSinW_W1aAcmavd7c0fkrwgmB9aDW6sc130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP676057.RAe9oSvz-MXgtoSinW_W1aAcmavd7c0fkrwgmB9aDW6sc130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP676057.RAe9oSvz-MXgtoSinW_W1aAcmavd7c0fkrwgmB9aDW6sc130_provenance.
- befree-20150227 importedOn "2015-02-27" NP676057.RAe9oSvz-MXgtoSinW_W1aAcmavd7c0fkrwgmB9aDW6sc130_provenance.
- NP676057.RAe9oSvz-MXgtoSinW_W1aAcmavd7c0fkrwgmB9aDW6sc130_assertion wasGeneratedBy ECO_0000203 NP676057.RAe9oSvz-MXgtoSinW_W1aAcmavd7c0fkrwgmB9aDW6sc130_provenance.
- NP676057.RAe9oSvz-MXgtoSinW_W1aAcmavd7c0fkrwgmB9aDW6sc130_assertion wasDerivedFrom befree-20150227 NP676057.RAe9oSvz-MXgtoSinW_W1aAcmavd7c0fkrwgmB9aDW6sc130_provenance.
- NP676057.RAe9oSvz-MXgtoSinW_W1aAcmavd7c0fkrwgmB9aDW6sc130_assertion SIO_000772 20569259 NP676057.RAe9oSvz-MXgtoSinW_W1aAcmavd7c0fkrwgmB9aDW6sc130_provenance.
- NP676057.RAe9oSvz-MXgtoSinW_W1aAcmavd7c0fkrwgmB9aDW6sc130_assertion evidence source_evidence_literature NP676057.RAe9oSvz-MXgtoSinW_W1aAcmavd7c0fkrwgmB9aDW6sc130_provenance.
- NP676057.RAe9oSvz-MXgtoSinW_W1aAcmavd7c0fkrwgmB9aDW6sc130_assertion description "[Thirty-four cases of SDS patients were analyzed and compared to other patients with the four most common IBMFSs on the CIMFS: Diamond Blackfan anemia, Fanconi anemia (FA), Kostmann/severe congenital neutropenia and dyskeratosis congenita (DC).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP676057.RAe9oSvz-MXgtoSinW_W1aAcmavd7c0fkrwgmB9aDW6sc130_provenance.