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- source_evidence_literature type ECO_0000212 NP288506.RAeBpqOczK10FYuzvg5AbEG4lPcz0wDTgC6GzyYUXrHs0130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP288506.RAeBpqOczK10FYuzvg5AbEG4lPcz0wDTgC6GzyYUXrHs0130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP288506.RAeBpqOczK10FYuzvg5AbEG4lPcz0wDTgC6GzyYUXrHs0130_provenance.
- NP288506.RAeBpqOczK10FYuzvg5AbEG4lPcz0wDTgC6GzyYUXrHs0130_assertion description "[Most Finnish patients with MGA1 carry the disease-specific P1297L mutation (FM1) in the IF-B(12) receptor, cubilin.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP288506.RAeBpqOczK10FYuzvg5AbEG4lPcz0wDTgC6GzyYUXrHs0130_provenance.
- NP288506.RAeBpqOczK10FYuzvg5AbEG4lPcz0wDTgC6GzyYUXrHs0130_assertion evidence source_evidence_literature NP288506.RAeBpqOczK10FYuzvg5AbEG4lPcz0wDTgC6GzyYUXrHs0130_provenance.
- NP288506.RAeBpqOczK10FYuzvg5AbEG4lPcz0wDTgC6GzyYUXrHs0130_assertion SIO_000772 10887099 NP288506.RAeBpqOczK10FYuzvg5AbEG4lPcz0wDTgC6GzyYUXrHs0130_provenance.
- NP288506.RAeBpqOczK10FYuzvg5AbEG4lPcz0wDTgC6GzyYUXrHs0130_assertion wasDerivedFrom befree-2016 NP288506.RAeBpqOczK10FYuzvg5AbEG4lPcz0wDTgC6GzyYUXrHs0130_provenance.
- NP288506.RAeBpqOczK10FYuzvg5AbEG4lPcz0wDTgC6GzyYUXrHs0130_assertion wasGeneratedBy ECO_0000203 NP288506.RAeBpqOczK10FYuzvg5AbEG4lPcz0wDTgC6GzyYUXrHs0130_provenance.
- befree-2016 importedOn "2016-02-19" NP288506.RAeBpqOczK10FYuzvg5AbEG4lPcz0wDTgC6GzyYUXrHs0130_provenance.