Matches in Nanopublications for { <http://rdf.disgenet.org/nanopublications.trig#NP178063.RAATGaxKTJVlIf8WTiXDKUr7ivqDB1Rm9DVKIXs7dNWgM130_assertion> ?p ?o ?g. }
Showing items 1 to 6 of
6
with 100 items per page.
- NP178063.RAATGaxKTJVlIf8WTiXDKUr7ivqDB1Rm9DVKIXs7dNWgM130_assertion type Assertion NP178063.RAATGaxKTJVlIf8WTiXDKUr7ivqDB1Rm9DVKIXs7dNWgM130_head.
- NP178063.RAATGaxKTJVlIf8WTiXDKUr7ivqDB1Rm9DVKIXs7dNWgM130_assertion description "[The autosomal dominant, giant-platelet disorders, May-Hegglin anomaly (MHA; MIM 155100), Fechtner syndrome (FTNS; MIM 153640) and Sebastian syndrome (SBS), share the triad of thrombocytopenia, large platelets and characteristic leukocyte inclusions ('D�hle-like' bodies).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP178063.RAATGaxKTJVlIf8WTiXDKUr7ivqDB1Rm9DVKIXs7dNWgM130_provenance.
- NP178063.RAATGaxKTJVlIf8WTiXDKUr7ivqDB1Rm9DVKIXs7dNWgM130_assertion evidence source_evidence_literature NP178063.RAATGaxKTJVlIf8WTiXDKUr7ivqDB1Rm9DVKIXs7dNWgM130_provenance.
- NP178063.RAATGaxKTJVlIf8WTiXDKUr7ivqDB1Rm9DVKIXs7dNWgM130_assertion SIO_000772 10973259 NP178063.RAATGaxKTJVlIf8WTiXDKUr7ivqDB1Rm9DVKIXs7dNWgM130_provenance.
- NP178063.RAATGaxKTJVlIf8WTiXDKUr7ivqDB1Rm9DVKIXs7dNWgM130_assertion wasDerivedFrom befree-20140225 NP178063.RAATGaxKTJVlIf8WTiXDKUr7ivqDB1Rm9DVKIXs7dNWgM130_provenance.
- NP178063.RAATGaxKTJVlIf8WTiXDKUr7ivqDB1Rm9DVKIXs7dNWgM130_assertion wasGeneratedBy ECO_0000203 NP178063.RAATGaxKTJVlIf8WTiXDKUr7ivqDB1Rm9DVKIXs7dNWgM130_provenance.