Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP273714.RA4LLfy8D_j6LI3Zgcn-MnTcLjKhm2nWcbTWaPk5z9Mlc130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP273714.RA4LLfy8D_j6LI3Zgcn-MnTcLjKhm2nWcbTWaPk5z9Mlc130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP273714.RA4LLfy8D_j6LI3Zgcn-MnTcLjKhm2nWcbTWaPk5z9Mlc130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP273714.RA4LLfy8D_j6LI3Zgcn-MnTcLjKhm2nWcbTWaPk5z9Mlc130_provenance.
- NP273714.RA4LLfy8D_j6LI3Zgcn-MnTcLjKhm2nWcbTWaPk5z9Mlc130_assertion description "[In this study we analyzed bone marrow and blood samples from 13 patients with myeloid leukemia (de novo myelodysplastic syndrome [MDS], n = 3; de novo acute myeloid leukemia [AML], n = 9; therapy-related (t-) AML, n = 1) which, on chromosome banding analysis, exhibited deletions (n = 12) or in one case a balanced translocation involving bands 7q31-qter using fluorescence in situ hybridization (FISH).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP273714.RA4LLfy8D_j6LI3Zgcn-MnTcLjKhm2nWcbTWaPk5z9Mlc130_provenance.
- NP273714.RA4LLfy8D_j6LI3Zgcn-MnTcLjKhm2nWcbTWaPk5z9Mlc130_assertion evidence source_evidence_literature NP273714.RA4LLfy8D_j6LI3Zgcn-MnTcLjKhm2nWcbTWaPk5z9Mlc130_provenance.
- NP273714.RA4LLfy8D_j6LI3Zgcn-MnTcLjKhm2nWcbTWaPk5z9Mlc130_assertion SIO_000772 9834205 NP273714.RA4LLfy8D_j6LI3Zgcn-MnTcLjKhm2nWcbTWaPk5z9Mlc130_provenance.
- NP273714.RA4LLfy8D_j6LI3Zgcn-MnTcLjKhm2nWcbTWaPk5z9Mlc130_assertion wasDerivedFrom befree-20140225 NP273714.RA4LLfy8D_j6LI3Zgcn-MnTcLjKhm2nWcbTWaPk5z9Mlc130_provenance.
- NP273714.RA4LLfy8D_j6LI3Zgcn-MnTcLjKhm2nWcbTWaPk5z9Mlc130_assertion wasGeneratedBy ECO_0000203 NP273714.RA4LLfy8D_j6LI3Zgcn-MnTcLjKhm2nWcbTWaPk5z9Mlc130_provenance.
- befree-20140225 importedOn "2014-02-25" NP273714.RA4LLfy8D_j6LI3Zgcn-MnTcLjKhm2nWcbTWaPk5z9Mlc130_provenance.