Matches in Nanopublications for { <http://rdf.disgenet.org/nanopublications.trig#NP903786.RAAZKgF7sx4MUIGoNFcaGVncN2Hv1B39xkvMVaLm1GL5g130_assertion> ?p ?o ?g. }
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- NP903786.RAAZKgF7sx4MUIGoNFcaGVncN2Hv1B39xkvMVaLm1GL5g130_assertion type Assertion NP903786.RAAZKgF7sx4MUIGoNFcaGVncN2Hv1B39xkvMVaLm1GL5g130_head.
- NP903786.RAAZKgF7sx4MUIGoNFcaGVncN2Hv1B39xkvMVaLm1GL5g130_assertion description "[Mutation of the non-muscle myosin heavy chain type II-A results in MYH9-related hereditary macrothrombocytopenia (HMTC), including four autosomal dominant platelet disorders: May-Hegglin anomaly (MHA), Sebastian (SBS), Fechtner (FS) and Epstein (EPS) syndrome.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP903786.RAAZKgF7sx4MUIGoNFcaGVncN2Hv1B39xkvMVaLm1GL5g130_provenance.
- NP903786.RAAZKgF7sx4MUIGoNFcaGVncN2Hv1B39xkvMVaLm1GL5g130_assertion evidence source_evidence_literature NP903786.RAAZKgF7sx4MUIGoNFcaGVncN2Hv1B39xkvMVaLm1GL5g130_provenance.
- NP903786.RAAZKgF7sx4MUIGoNFcaGVncN2Hv1B39xkvMVaLm1GL5g130_assertion SIO_000772 16098078 NP903786.RAAZKgF7sx4MUIGoNFcaGVncN2Hv1B39xkvMVaLm1GL5g130_provenance.
- NP903786.RAAZKgF7sx4MUIGoNFcaGVncN2Hv1B39xkvMVaLm1GL5g130_assertion wasDerivedFrom befree-20140225 NP903786.RAAZKgF7sx4MUIGoNFcaGVncN2Hv1B39xkvMVaLm1GL5g130_provenance.
- NP903786.RAAZKgF7sx4MUIGoNFcaGVncN2Hv1B39xkvMVaLm1GL5g130_assertion wasGeneratedBy ECO_0000203 NP903786.RAAZKgF7sx4MUIGoNFcaGVncN2Hv1B39xkvMVaLm1GL5g130_provenance.