Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP601020.RAWBRW77VxGkn96eCB3ormb4V0jNV8c6RW4qoJ9oLkMJM130_assertion> ?p ?o ?g. }
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- NP601020.RAWBRW77VxGkn96eCB3ormb4V0jNV8c6RW4qoJ9oLkMJM130_assertion type Assertion NP601020.RAWBRW77VxGkn96eCB3ormb4V0jNV8c6RW4qoJ9oLkMJM130_head.
- NP601020.RAWBRW77VxGkn96eCB3ormb4V0jNV8c6RW4qoJ9oLkMJM130_assertion wasGeneratedBy ECO_0000203 NP601020.RAWBRW77VxGkn96eCB3ormb4V0jNV8c6RW4qoJ9oLkMJM130_provenance.
- NP601020.RAWBRW77VxGkn96eCB3ormb4V0jNV8c6RW4qoJ9oLkMJM130_assertion wasDerivedFrom befree-20150227 NP601020.RAWBRW77VxGkn96eCB3ormb4V0jNV8c6RW4qoJ9oLkMJM130_provenance.
- NP601020.RAWBRW77VxGkn96eCB3ormb4V0jNV8c6RW4qoJ9oLkMJM130_assertion SIO_000772 17442773 NP601020.RAWBRW77VxGkn96eCB3ormb4V0jNV8c6RW4qoJ9oLkMJM130_provenance.
- NP601020.RAWBRW77VxGkn96eCB3ormb4V0jNV8c6RW4qoJ9oLkMJM130_assertion evidence source_evidence_literature NP601020.RAWBRW77VxGkn96eCB3ormb4V0jNV8c6RW4qoJ9oLkMJM130_provenance.
- NP601020.RAWBRW77VxGkn96eCB3ormb4V0jNV8c6RW4qoJ9oLkMJM130_assertion description "[Analysis of NUP98 allelic expression in AML and myelodysplastic syndrome showed loss of heterozygosity observed in 29% of the former and 8% of the latter.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP601020.RAWBRW77VxGkn96eCB3ormb4V0jNV8c6RW4qoJ9oLkMJM130_provenance.