Matches in Nanopublications for { <http://rdf.disgenet.org/nanopublications.trig#NP318423.RAPSDf0dYy3DfKkb2CPthaAi9DNQPzkwzR9ZbxB9CNbPc130_assertion> ?p ?o ?g. }
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- NP318423.RAPSDf0dYy3DfKkb2CPthaAi9DNQPzkwzR9ZbxB9CNbPc130_assertion type Assertion NP318423.RAPSDf0dYy3DfKkb2CPthaAi9DNQPzkwzR9ZbxB9CNbPc130_head.
- NP318423.RAPSDf0dYy3DfKkb2CPthaAi9DNQPzkwzR9ZbxB9CNbPc130_assertion description "[Mutations in CSF3R are common in patients with CNL or atypical CML and represent a potentially useful criterion for diagnosing these neoplasms.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP318423.RAPSDf0dYy3DfKkb2CPthaAi9DNQPzkwzR9ZbxB9CNbPc130_provenance.
- NP318423.RAPSDf0dYy3DfKkb2CPthaAi9DNQPzkwzR9ZbxB9CNbPc130_assertion evidence source_evidence_literature NP318423.RAPSDf0dYy3DfKkb2CPthaAi9DNQPzkwzR9ZbxB9CNbPc130_provenance.
- NP318423.RAPSDf0dYy3DfKkb2CPthaAi9DNQPzkwzR9ZbxB9CNbPc130_assertion SIO_000772 23656643 NP318423.RAPSDf0dYy3DfKkb2CPthaAi9DNQPzkwzR9ZbxB9CNbPc130_provenance.
- NP318423.RAPSDf0dYy3DfKkb2CPthaAi9DNQPzkwzR9ZbxB9CNbPc130_assertion wasDerivedFrom befree-20140225 NP318423.RAPSDf0dYy3DfKkb2CPthaAi9DNQPzkwzR9ZbxB9CNbPc130_provenance.
- NP318423.RAPSDf0dYy3DfKkb2CPthaAi9DNQPzkwzR9ZbxB9CNbPc130_assertion wasGeneratedBy ECO_0000203 NP318423.RAPSDf0dYy3DfKkb2CPthaAi9DNQPzkwzR9ZbxB9CNbPc130_provenance.