Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP1378991.RAcquLRvH0YMmTGzeS5aKvZjfp0FTa2VN3argQ2dcBdos130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP1378991.RAcquLRvH0YMmTGzeS5aKvZjfp0FTa2VN3argQ2dcBdos130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP1378991.RAcquLRvH0YMmTGzeS5aKvZjfp0FTa2VN3argQ2dcBdos130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP1378991.RAcquLRvH0YMmTGzeS5aKvZjfp0FTa2VN3argQ2dcBdos130_provenance.
- befree-2016 importedOn "2016-02-19" NP1378991.RAcquLRvH0YMmTGzeS5aKvZjfp0FTa2VN3argQ2dcBdos130_provenance.
- NP1378991.RAcquLRvH0YMmTGzeS5aKvZjfp0FTa2VN3argQ2dcBdos130_assertion wasGeneratedBy ECO_0000203 NP1378991.RAcquLRvH0YMmTGzeS5aKvZjfp0FTa2VN3argQ2dcBdos130_provenance.
- NP1378991.RAcquLRvH0YMmTGzeS5aKvZjfp0FTa2VN3argQ2dcBdos130_assertion wasDerivedFrom befree-2016 NP1378991.RAcquLRvH0YMmTGzeS5aKvZjfp0FTa2VN3argQ2dcBdos130_provenance.
- NP1378991.RAcquLRvH0YMmTGzeS5aKvZjfp0FTa2VN3argQ2dcBdos130_assertion SIO_000772 9264367 NP1378991.RAcquLRvH0YMmTGzeS5aKvZjfp0FTa2VN3argQ2dcBdos130_provenance.
- NP1378991.RAcquLRvH0YMmTGzeS5aKvZjfp0FTa2VN3argQ2dcBdos130_assertion evidence source_evidence_literature NP1378991.RAcquLRvH0YMmTGzeS5aKvZjfp0FTa2VN3argQ2dcBdos130_provenance.
- NP1378991.RAcquLRvH0YMmTGzeS5aKvZjfp0FTa2VN3argQ2dcBdos130_assertion description "[Deletions of the long arm of chromosome 5 with common overlapping segment 5q31.1 are among the most frequent cytogenetic aberrations in myelodysplastic syndromes and acute myeloid leukemias (MDS/AML).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1378991.RAcquLRvH0YMmTGzeS5aKvZjfp0FTa2VN3argQ2dcBdos130_provenance.