Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP300947.RA_e8v62MD_zOFC11W1VJ21eP94zy0pgtVsMzMPFlj2E4130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP300947.RA_e8v62MD_zOFC11W1VJ21eP94zy0pgtVsMzMPFlj2E4130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP300947.RA_e8v62MD_zOFC11W1VJ21eP94zy0pgtVsMzMPFlj2E4130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP300947.RA_e8v62MD_zOFC11W1VJ21eP94zy0pgtVsMzMPFlj2E4130_provenance.
- NP300947.RA_e8v62MD_zOFC11W1VJ21eP94zy0pgtVsMzMPFlj2E4130_assertion description "[To determine if CDKN2 or another closely related gene on 9p is the target of 9p deletions in ALL and other hematologic malignancies, we analyzed 20 primary patient samples (13 ALL, 2 acute myeloid leukemias [AML], and 5 non-Hodgkin's lymphomas [NHL]) with 9p rearrangements using Southern blot analysis, fluorescence in situ hybridization (FISH), and single-strand conformation polymorphism (SSCP) for alterations of CDKN2.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP300947.RA_e8v62MD_zOFC11W1VJ21eP94zy0pgtVsMzMPFlj2E4130_provenance.
- NP300947.RA_e8v62MD_zOFC11W1VJ21eP94zy0pgtVsMzMPFlj2E4130_assertion evidence source_evidence_literature NP300947.RA_e8v62MD_zOFC11W1VJ21eP94zy0pgtVsMzMPFlj2E4130_provenance.
- NP300947.RA_e8v62MD_zOFC11W1VJ21eP94zy0pgtVsMzMPFlj2E4130_assertion SIO_000772 7544647 NP300947.RA_e8v62MD_zOFC11W1VJ21eP94zy0pgtVsMzMPFlj2E4130_provenance.
- NP300947.RA_e8v62MD_zOFC11W1VJ21eP94zy0pgtVsMzMPFlj2E4130_assertion wasDerivedFrom befree-20150227 NP300947.RA_e8v62MD_zOFC11W1VJ21eP94zy0pgtVsMzMPFlj2E4130_provenance.
- NP300947.RA_e8v62MD_zOFC11W1VJ21eP94zy0pgtVsMzMPFlj2E4130_assertion wasGeneratedBy ECO_0000203 NP300947.RA_e8v62MD_zOFC11W1VJ21eP94zy0pgtVsMzMPFlj2E4130_provenance.
- befree-20150227 importedOn "2015-02-27" NP300947.RA_e8v62MD_zOFC11W1VJ21eP94zy0pgtVsMzMPFlj2E4130_provenance.