Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP587982.RAQL8cvYRIqsnxsAmedCrjzy3ZsyFHMzOnw8v7r41oyZc130_assertion> ?p ?o ?g. }
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- NP587982.RAQL8cvYRIqsnxsAmedCrjzy3ZsyFHMzOnw8v7r41oyZc130_assertion type Assertion NP587982.RAQL8cvYRIqsnxsAmedCrjzy3ZsyFHMzOnw8v7r41oyZc130_head.
- NP587982.RAQL8cvYRIqsnxsAmedCrjzy3ZsyFHMzOnw8v7r41oyZc130_assertion description "[We report a patient with myelodysplastic syndrome (refractory anemia) showing the karyotype 46,XY,+1,der(1;10)(q10;p10), resulting in trisomy 1q and monosomy 10q abnormality.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP587982.RAQL8cvYRIqsnxsAmedCrjzy3ZsyFHMzOnw8v7r41oyZc130_provenance.
- NP587982.RAQL8cvYRIqsnxsAmedCrjzy3ZsyFHMzOnw8v7r41oyZc130_assertion evidence source_evidence_literature NP587982.RAQL8cvYRIqsnxsAmedCrjzy3ZsyFHMzOnw8v7r41oyZc130_provenance.
- NP587982.RAQL8cvYRIqsnxsAmedCrjzy3ZsyFHMzOnw8v7r41oyZc130_assertion SIO_000772 17213027 NP587982.RAQL8cvYRIqsnxsAmedCrjzy3ZsyFHMzOnw8v7r41oyZc130_provenance.
- NP587982.RAQL8cvYRIqsnxsAmedCrjzy3ZsyFHMzOnw8v7r41oyZc130_assertion wasDerivedFrom befree-2016 NP587982.RAQL8cvYRIqsnxsAmedCrjzy3ZsyFHMzOnw8v7r41oyZc130_provenance.
- NP587982.RAQL8cvYRIqsnxsAmedCrjzy3ZsyFHMzOnw8v7r41oyZc130_assertion wasGeneratedBy ECO_0000203 NP587982.RAQL8cvYRIqsnxsAmedCrjzy3ZsyFHMzOnw8v7r41oyZc130_provenance.