Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP914012.RAEt1k4BjxNYdU2eRgsl-EWFWCSnyEJKzRtKMp8tbzTbg130_assertion> ?p ?o ?g. }
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- NP914012.RAEt1k4BjxNYdU2eRgsl-EWFWCSnyEJKzRtKMp8tbzTbg130_assertion type Assertion NP914012.RAEt1k4BjxNYdU2eRgsl-EWFWCSnyEJKzRtKMp8tbzTbg130_head.
- NP914012.RAEt1k4BjxNYdU2eRgsl-EWFWCSnyEJKzRtKMp8tbzTbg130_assertion description "[Cases with familial monosomy 7 are well recognized, but there are no reports of familial MDS with deletion of 5q.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP914012.RAEt1k4BjxNYdU2eRgsl-EWFWCSnyEJKzRtKMp8tbzTbg130_provenance.
- NP914012.RAEt1k4BjxNYdU2eRgsl-EWFWCSnyEJKzRtKMp8tbzTbg130_assertion evidence source_evidence_literature NP914012.RAEt1k4BjxNYdU2eRgsl-EWFWCSnyEJKzRtKMp8tbzTbg130_provenance.
- NP914012.RAEt1k4BjxNYdU2eRgsl-EWFWCSnyEJKzRtKMp8tbzTbg130_assertion SIO_000772 8217806 NP914012.RAEt1k4BjxNYdU2eRgsl-EWFWCSnyEJKzRtKMp8tbzTbg130_provenance.
- NP914012.RAEt1k4BjxNYdU2eRgsl-EWFWCSnyEJKzRtKMp8tbzTbg130_assertion wasDerivedFrom befree-20150227 NP914012.RAEt1k4BjxNYdU2eRgsl-EWFWCSnyEJKzRtKMp8tbzTbg130_provenance.
- NP914012.RAEt1k4BjxNYdU2eRgsl-EWFWCSnyEJKzRtKMp8tbzTbg130_assertion wasGeneratedBy ECO_0000203 NP914012.RAEt1k4BjxNYdU2eRgsl-EWFWCSnyEJKzRtKMp8tbzTbg130_provenance.