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- source_evidence_literature type ECO_0000212 NP581022.RAnWp-waMIRqmhmRkagwYu9O8VTm_qs2ShYBoN4wZaIhA130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP581022.RAnWp-waMIRqmhmRkagwYu9O8VTm_qs2ShYBoN4wZaIhA130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP581022.RAnWp-waMIRqmhmRkagwYu9O8VTm_qs2ShYBoN4wZaIhA130_provenance.
- NP581022.RAnWp-waMIRqmhmRkagwYu9O8VTm_qs2ShYBoN4wZaIhA130_assertion description "[A novel MLH1 mutation harbored as a germ line aberration by a young woman of an HNPCC-like family and exhibited by a CML patient when occurring prior to the initiation of the blast phase concomitant with a c-MYC amplification.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP581022.RAnWp-waMIRqmhmRkagwYu9O8VTm_qs2ShYBoN4wZaIhA130_provenance.
- NP581022.RAnWp-waMIRqmhmRkagwYu9O8VTm_qs2ShYBoN4wZaIhA130_assertion evidence source_evidence_literature NP581022.RAnWp-waMIRqmhmRkagwYu9O8VTm_qs2ShYBoN4wZaIhA130_provenance.
- NP581022.RAnWp-waMIRqmhmRkagwYu9O8VTm_qs2ShYBoN4wZaIhA130_assertion SIO_000772 16685411 NP581022.RAnWp-waMIRqmhmRkagwYu9O8VTm_qs2ShYBoN4wZaIhA130_provenance.
- NP581022.RAnWp-waMIRqmhmRkagwYu9O8VTm_qs2ShYBoN4wZaIhA130_assertion wasDerivedFrom befree-20150227 NP581022.RAnWp-waMIRqmhmRkagwYu9O8VTm_qs2ShYBoN4wZaIhA130_provenance.
- NP581022.RAnWp-waMIRqmhmRkagwYu9O8VTm_qs2ShYBoN4wZaIhA130_assertion wasGeneratedBy ECO_0000203 NP581022.RAnWp-waMIRqmhmRkagwYu9O8VTm_qs2ShYBoN4wZaIhA130_provenance.
- befree-20150227 importedOn "2015-02-27" NP581022.RAnWp-waMIRqmhmRkagwYu9O8VTm_qs2ShYBoN4wZaIhA130_provenance.