Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP140520.RAa13pSDRpuvB3J6HEsVBJLgmaP1kl2YNc3zYxQEhRVj8130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP140520.RAa13pSDRpuvB3J6HEsVBJLgmaP1kl2YNc3zYxQEhRVj8130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP140520.RAa13pSDRpuvB3J6HEsVBJLgmaP1kl2YNc3zYxQEhRVj8130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP140520.RAa13pSDRpuvB3J6HEsVBJLgmaP1kl2YNc3zYxQEhRVj8130_provenance.
- NP140520.RAa13pSDRpuvB3J6HEsVBJLgmaP1kl2YNc3zYxQEhRVj8130_assertion description "[Mutations in CLN7/MFSD8 are a common cause of variant late-infantile neuronal ceroid lipofuscinosis.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP140520.RAa13pSDRpuvB3J6HEsVBJLgmaP1kl2YNc3zYxQEhRVj8130_provenance.
- NP140520.RAa13pSDRpuvB3J6HEsVBJLgmaP1kl2YNc3zYxQEhRVj8130_assertion evidence source_evidence_literature NP140520.RAa13pSDRpuvB3J6HEsVBJLgmaP1kl2YNc3zYxQEhRVj8130_provenance.
- NP140520.RAa13pSDRpuvB3J6HEsVBJLgmaP1kl2YNc3zYxQEhRVj8130_assertion SIO_000772 19201763 NP140520.RAa13pSDRpuvB3J6HEsVBJLgmaP1kl2YNc3zYxQEhRVj8130_provenance.
- NP140520.RAa13pSDRpuvB3J6HEsVBJLgmaP1kl2YNc3zYxQEhRVj8130_assertion wasDerivedFrom gad-20150221 NP140520.RAa13pSDRpuvB3J6HEsVBJLgmaP1kl2YNc3zYxQEhRVj8130_provenance.
- NP140520.RAa13pSDRpuvB3J6HEsVBJLgmaP1kl2YNc3zYxQEhRVj8130_assertion wasGeneratedBy ECO_0000203 NP140520.RAa13pSDRpuvB3J6HEsVBJLgmaP1kl2YNc3zYxQEhRVj8130_provenance.
- gad-20150221 importedOn "2015-02-21" NP140520.RAa13pSDRpuvB3J6HEsVBJLgmaP1kl2YNc3zYxQEhRVj8130_provenance.