Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP394388.RAVlEVRoq1uL7PFUb3rkLyhP5nSdE7kp3BbeX3XoTS0NU130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP394388.RAVlEVRoq1uL7PFUb3rkLyhP5nSdE7kp3BbeX3XoTS0NU130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP394388.RAVlEVRoq1uL7PFUb3rkLyhP5nSdE7kp3BbeX3XoTS0NU130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP394388.RAVlEVRoq1uL7PFUb3rkLyhP5nSdE7kp3BbeX3XoTS0NU130_provenance.
- NP394388.RAVlEVRoq1uL7PFUb3rkLyhP5nSdE7kp3BbeX3XoTS0NU130_assertion description "[A patient with ANLL FAB subtype M1 was found to possess a t(16;21)(p11;q22) and trisomy 10.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP394388.RAVlEVRoq1uL7PFUb3rkLyhP5nSdE7kp3BbeX3XoTS0NU130_provenance.
- NP394388.RAVlEVRoq1uL7PFUb3rkLyhP5nSdE7kp3BbeX3XoTS0NU130_assertion evidence source_evidence_literature NP394388.RAVlEVRoq1uL7PFUb3rkLyhP5nSdE7kp3BbeX3XoTS0NU130_provenance.
- NP394388.RAVlEVRoq1uL7PFUb3rkLyhP5nSdE7kp3BbeX3XoTS0NU130_assertion SIO_000772 8242597 NP394388.RAVlEVRoq1uL7PFUb3rkLyhP5nSdE7kp3BbeX3XoTS0NU130_provenance.
- NP394388.RAVlEVRoq1uL7PFUb3rkLyhP5nSdE7kp3BbeX3XoTS0NU130_assertion wasDerivedFrom befree-20150227 NP394388.RAVlEVRoq1uL7PFUb3rkLyhP5nSdE7kp3BbeX3XoTS0NU130_provenance.
- NP394388.RAVlEVRoq1uL7PFUb3rkLyhP5nSdE7kp3BbeX3XoTS0NU130_assertion wasGeneratedBy ECO_0000203 NP394388.RAVlEVRoq1uL7PFUb3rkLyhP5nSdE7kp3BbeX3XoTS0NU130_provenance.
- befree-20150227 importedOn "2015-02-27" NP394388.RAVlEVRoq1uL7PFUb3rkLyhP5nSdE7kp3BbeX3XoTS0NU130_provenance.