Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP332171.RAcB44cZpdcsQxAGEd8LrcG6s3KbFNiLczW2UiJzvyQBs130_assertion> ?p ?o ?g. }
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- NP332171.RAcB44cZpdcsQxAGEd8LrcG6s3KbFNiLczW2UiJzvyQBs130_assertion type Assertion NP332171.RAcB44cZpdcsQxAGEd8LrcG6s3KbFNiLczW2UiJzvyQBs130_head.
- NP332171.RAcB44cZpdcsQxAGEd8LrcG6s3KbFNiLczW2UiJzvyQBs130_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." NP332171.RAcB44cZpdcsQxAGEd8LrcG6s3KbFNiLczW2UiJzvyQBs130_provenance.
- NP332171.RAcB44cZpdcsQxAGEd8LrcG6s3KbFNiLczW2UiJzvyQBs130_assertion evidence source_evidence_literature NP332171.RAcB44cZpdcsQxAGEd8LrcG6s3KbFNiLczW2UiJzvyQBs130_provenance.
- NP332171.RAcB44cZpdcsQxAGEd8LrcG6s3KbFNiLczW2UiJzvyQBs130_assertion SIO_000772 23656643 NP332171.RAcB44cZpdcsQxAGEd8LrcG6s3KbFNiLczW2UiJzvyQBs130_provenance.
- NP332171.RAcB44cZpdcsQxAGEd8LrcG6s3KbFNiLczW2UiJzvyQBs130_assertion wasDerivedFrom befree-20150227 NP332171.RAcB44cZpdcsQxAGEd8LrcG6s3KbFNiLczW2UiJzvyQBs130_provenance.
- NP332171.RAcB44cZpdcsQxAGEd8LrcG6s3KbFNiLczW2UiJzvyQBs130_assertion wasGeneratedBy ECO_0000203 NP332171.RAcB44cZpdcsQxAGEd8LrcG6s3KbFNiLczW2UiJzvyQBs130_provenance.