Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP569732.RARfytfa1QjRRQUuydUiJoHzwW_DALrfmgQs1GsHeal_c130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP569732.RARfytfa1QjRRQUuydUiJoHzwW_DALrfmgQs1GsHeal_c130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP569732.RARfytfa1QjRRQUuydUiJoHzwW_DALrfmgQs1GsHeal_c130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP569732.RARfytfa1QjRRQUuydUiJoHzwW_DALrfmgQs1GsHeal_c130_provenance.
- NP569732.RARfytfa1QjRRQUuydUiJoHzwW_DALrfmgQs1GsHeal_c130_assertion description "[To conclude, our data suggest that the V(H) mutation frequency in mantle cell lymphoma may be higher than previously believed.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP569732.RARfytfa1QjRRQUuydUiJoHzwW_DALrfmgQs1GsHeal_c130_provenance.
- NP569732.RARfytfa1QjRRQUuydUiJoHzwW_DALrfmgQs1GsHeal_c130_assertion evidence source_evidence_literature NP569732.RARfytfa1QjRRQUuydUiJoHzwW_DALrfmgQs1GsHeal_c130_provenance.
- NP569732.RARfytfa1QjRRQUuydUiJoHzwW_DALrfmgQs1GsHeal_c130_assertion SIO_000772 16980950 NP569732.RARfytfa1QjRRQUuydUiJoHzwW_DALrfmgQs1GsHeal_c130_provenance.
- NP569732.RARfytfa1QjRRQUuydUiJoHzwW_DALrfmgQs1GsHeal_c130_assertion wasDerivedFrom befree-2016 NP569732.RARfytfa1QjRRQUuydUiJoHzwW_DALrfmgQs1GsHeal_c130_provenance.
- NP569732.RARfytfa1QjRRQUuydUiJoHzwW_DALrfmgQs1GsHeal_c130_assertion wasGeneratedBy ECO_0000203 NP569732.RARfytfa1QjRRQUuydUiJoHzwW_DALrfmgQs1GsHeal_c130_provenance.
- befree-2016 importedOn "2016-02-19" NP569732.RARfytfa1QjRRQUuydUiJoHzwW_DALrfmgQs1GsHeal_c130_provenance.