Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP1248308.RANAslNq8-J9cNlfK8kl405Y341TolZq-51Kv6aUZZkZI130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP1248308.RANAslNq8-J9cNlfK8kl405Y341TolZq-51Kv6aUZZkZI130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP1248308.RANAslNq8-J9cNlfK8kl405Y341TolZq-51Kv6aUZZkZI130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP1248308.RANAslNq8-J9cNlfK8kl405Y341TolZq-51Kv6aUZZkZI130_provenance.
- NP1248308.RANAslNq8-J9cNlfK8kl405Y341TolZq-51Kv6aUZZkZI130_assertion description "[Cytogenetic and flow cytometry evaluation of Richter syndrome reveals MYC, CDKN2A, IGH alterations with loss of CD52, CD62L and increase of CD71 antigen expression as the most frequent recurrent abnormalities.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1248308.RANAslNq8-J9cNlfK8kl405Y341TolZq-51Kv6aUZZkZI130_provenance.
- NP1248308.RANAslNq8-J9cNlfK8kl405Y341TolZq-51Kv6aUZZkZI130_assertion evidence source_evidence_literature NP1248308.RANAslNq8-J9cNlfK8kl405Y341TolZq-51Kv6aUZZkZI130_provenance.
- NP1248308.RANAslNq8-J9cNlfK8kl405Y341TolZq-51Kv6aUZZkZI130_assertion SIO_000772 25511139 NP1248308.RANAslNq8-J9cNlfK8kl405Y341TolZq-51Kv6aUZZkZI130_provenance.
- NP1248308.RANAslNq8-J9cNlfK8kl405Y341TolZq-51Kv6aUZZkZI130_assertion wasDerivedFrom befree-2016 NP1248308.RANAslNq8-J9cNlfK8kl405Y341TolZq-51Kv6aUZZkZI130_provenance.
- NP1248308.RANAslNq8-J9cNlfK8kl405Y341TolZq-51Kv6aUZZkZI130_assertion wasGeneratedBy ECO_0000203 NP1248308.RANAslNq8-J9cNlfK8kl405Y341TolZq-51Kv6aUZZkZI130_provenance.
- befree-2016 importedOn "2016-02-19" NP1248308.RANAslNq8-J9cNlfK8kl405Y341TolZq-51Kv6aUZZkZI130_provenance.