Matches in Nanopublications for { <http://rdf.disgenet.org/nanopublications.trig#NP427768.RAxLF0xd5aIoVf6kQCsUWB1ofymghvXpogTTHuz35DvXc130_assertion> ?p ?o ?g. }
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- NP427768.RAxLF0xd5aIoVf6kQCsUWB1ofymghvXpogTTHuz35DvXc130_assertion type Assertion NP427768.RAxLF0xd5aIoVf6kQCsUWB1ofymghvXpogTTHuz35DvXc130_head.
- NP427768.RAxLF0xd5aIoVf6kQCsUWB1ofymghvXpogTTHuz35DvXc130_assertion description "[Mutations in SETBP1 are recurrent in myelodysplastic syndromes and often coexist with cytogenetic markers associated with disease progression.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP427768.RAxLF0xd5aIoVf6kQCsUWB1ofymghvXpogTTHuz35DvXc130_provenance.
- NP427768.RAxLF0xd5aIoVf6kQCsUWB1ofymghvXpogTTHuz35DvXc130_assertion evidence source_evidence_literature NP427768.RAxLF0xd5aIoVf6kQCsUWB1ofymghvXpogTTHuz35DvXc130_provenance.
- NP427768.RAxLF0xd5aIoVf6kQCsUWB1ofymghvXpogTTHuz35DvXc130_assertion SIO_000772 23889083 NP427768.RAxLF0xd5aIoVf6kQCsUWB1ofymghvXpogTTHuz35DvXc130_provenance.
- NP427768.RAxLF0xd5aIoVf6kQCsUWB1ofymghvXpogTTHuz35DvXc130_assertion wasDerivedFrom befree-20140225 NP427768.RAxLF0xd5aIoVf6kQCsUWB1ofymghvXpogTTHuz35DvXc130_provenance.
- NP427768.RAxLF0xd5aIoVf6kQCsUWB1ofymghvXpogTTHuz35DvXc130_assertion wasGeneratedBy ECO_0000203 NP427768.RAxLF0xd5aIoVf6kQCsUWB1ofymghvXpogTTHuz35DvXc130_provenance.