Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP605896.RAkUvSTegM3tEaICt7TA0CeryMjTh5Lm94dg0FmTFAU48130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP605896.RAkUvSTegM3tEaICt7TA0CeryMjTh5Lm94dg0FmTFAU48130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP605896.RAkUvSTegM3tEaICt7TA0CeryMjTh5Lm94dg0FmTFAU48130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP605896.RAkUvSTegM3tEaICt7TA0CeryMjTh5Lm94dg0FmTFAU48130_provenance.
- NP605896.RAkUvSTegM3tEaICt7TA0CeryMjTh5Lm94dg0FmTFAU48130_assertion description "[Focusing on cytogenetic aberrations most commonly found in MDS, we retrospectively genotyped 566 MDS/AML patients carrying -5/del(5q), -7/del(7q), +8, del(20q) and -Y.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP605896.RAkUvSTegM3tEaICt7TA0CeryMjTh5Lm94dg0FmTFAU48130_provenance.
- NP605896.RAkUvSTegM3tEaICt7TA0CeryMjTh5Lm94dg0FmTFAU48130_assertion evidence source_evidence_literature NP605896.RAkUvSTegM3tEaICt7TA0CeryMjTh5Lm94dg0FmTFAU48130_provenance.
- NP605896.RAkUvSTegM3tEaICt7TA0CeryMjTh5Lm94dg0FmTFAU48130_assertion SIO_000772 23643325 NP605896.RAkUvSTegM3tEaICt7TA0CeryMjTh5Lm94dg0FmTFAU48130_provenance.
- NP605896.RAkUvSTegM3tEaICt7TA0CeryMjTh5Lm94dg0FmTFAU48130_assertion wasDerivedFrom befree-20150227 NP605896.RAkUvSTegM3tEaICt7TA0CeryMjTh5Lm94dg0FmTFAU48130_provenance.
- NP605896.RAkUvSTegM3tEaICt7TA0CeryMjTh5Lm94dg0FmTFAU48130_assertion wasGeneratedBy ECO_0000203 NP605896.RAkUvSTegM3tEaICt7TA0CeryMjTh5Lm94dg0FmTFAU48130_provenance.
- befree-20150227 importedOn "2015-02-27" NP605896.RAkUvSTegM3tEaICt7TA0CeryMjTh5Lm94dg0FmTFAU48130_provenance.