Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP188690.RAbe80s3gfDv_SYHcS7ZEzKq1cuFFeELhEIxP4UnPLMhA130_assertion> ?p ?o ?g. }
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- NP188690.RAbe80s3gfDv_SYHcS7ZEzKq1cuFFeELhEIxP4UnPLMhA130_assertion type Assertion NP188690.RAbe80s3gfDv_SYHcS7ZEzKq1cuFFeELhEIxP4UnPLMhA130_head.
- NP188690.RAbe80s3gfDv_SYHcS7ZEzKq1cuFFeELhEIxP4UnPLMhA130_assertion wasGeneratedBy ECO_0000203 NP188690.RAbe80s3gfDv_SYHcS7ZEzKq1cuFFeELhEIxP4UnPLMhA130_provenance.
- NP188690.RAbe80s3gfDv_SYHcS7ZEzKq1cuFFeELhEIxP4UnPLMhA130_assertion wasDerivedFrom lhgdn-20090331 NP188690.RAbe80s3gfDv_SYHcS7ZEzKq1cuFFeELhEIxP4UnPLMhA130_provenance.
- NP188690.RAbe80s3gfDv_SYHcS7ZEzKq1cuFFeELhEIxP4UnPLMhA130_assertion SIO_000772 15886296 NP188690.RAbe80s3gfDv_SYHcS7ZEzKq1cuFFeELhEIxP4UnPLMhA130_provenance.
- NP188690.RAbe80s3gfDv_SYHcS7ZEzKq1cuFFeELhEIxP4UnPLMhA130_assertion evidence source_evidence_literature NP188690.RAbe80s3gfDv_SYHcS7ZEzKq1cuFFeELhEIxP4UnPLMhA130_provenance.
- NP188690.RAbe80s3gfDv_SYHcS7ZEzKq1cuFFeELhEIxP4UnPLMhA130_assertion description "[FANCD2 mutations were also common in Microsatellite instability+ Therapy-related acute myeloid leukemia/myelodysplastic syndrome]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP188690.RAbe80s3gfDv_SYHcS7ZEzKq1cuFFeELhEIxP4UnPLMhA130_provenance.