Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP660450.RAiCK6duFucSdGXrsUp182zBo9BV5DakZxRxaV80iE43U130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP660450.RAiCK6duFucSdGXrsUp182zBo9BV5DakZxRxaV80iE43U130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP660450.RAiCK6duFucSdGXrsUp182zBo9BV5DakZxRxaV80iE43U130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP660450.RAiCK6duFucSdGXrsUp182zBo9BV5DakZxRxaV80iE43U130_provenance.
- NP660450.RAiCK6duFucSdGXrsUp182zBo9BV5DakZxRxaV80iE43U130_assertion description "[Moreover, tissue-specific knock-in of Ptpn11(E76K/+) mutation in lineage-committed myeloid, T lymphoid, and B lymphoid progenitors also results in AML, T-ALL, and B-ALL, respectively.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP660450.RAiCK6duFucSdGXrsUp182zBo9BV5DakZxRxaV80iE43U130_provenance.
- NP660450.RAiCK6duFucSdGXrsUp182zBo9BV5DakZxRxaV80iE43U130_assertion evidence source_evidence_literature NP660450.RAiCK6duFucSdGXrsUp182zBo9BV5DakZxRxaV80iE43U130_provenance.
- NP660450.RAiCK6duFucSdGXrsUp182zBo9BV5DakZxRxaV80iE43U130_assertion SIO_000772 21930766 NP660450.RAiCK6duFucSdGXrsUp182zBo9BV5DakZxRxaV80iE43U130_provenance.
- NP660450.RAiCK6duFucSdGXrsUp182zBo9BV5DakZxRxaV80iE43U130_assertion wasDerivedFrom befree-20150227 NP660450.RAiCK6duFucSdGXrsUp182zBo9BV5DakZxRxaV80iE43U130_provenance.
- NP660450.RAiCK6duFucSdGXrsUp182zBo9BV5DakZxRxaV80iE43U130_assertion wasGeneratedBy ECO_0000203 NP660450.RAiCK6duFucSdGXrsUp182zBo9BV5DakZxRxaV80iE43U130_provenance.
- befree-20150227 importedOn "2015-02-27" NP660450.RAiCK6duFucSdGXrsUp182zBo9BV5DakZxRxaV80iE43U130_provenance.