Matches in Nanopublications for { <http://rdf.disgenet.org/nanopublications.trig#NP616757.RAGtq_fcw6TIIWozo-xJNZPiYjVkAf-PtoTkroAwE8Qt4130_assertion> ?p ?o ?g. }
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- NP616757.RAGtq_fcw6TIIWozo-xJNZPiYjVkAf-PtoTkroAwE8Qt4130_assertion type Assertion NP616757.RAGtq_fcw6TIIWozo-xJNZPiYjVkAf-PtoTkroAwE8Qt4130_head.
- NP616757.RAGtq_fcw6TIIWozo-xJNZPiYjVkAf-PtoTkroAwE8Qt4130_assertion description "[Currently, MHA, SBS, FTNS and EPS are considered to be distinct clinical manifestation of a single illness caused by mutations of the MYH9 gene encoding the heavy chain of non-muscle myosin IIA (NMMHC-IIA).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP616757.RAGtq_fcw6TIIWozo-xJNZPiYjVkAf-PtoTkroAwE8Qt4130_provenance.
- NP616757.RAGtq_fcw6TIIWozo-xJNZPiYjVkAf-PtoTkroAwE8Qt4130_assertion evidence source_evidence_literature NP616757.RAGtq_fcw6TIIWozo-xJNZPiYjVkAf-PtoTkroAwE8Qt4130_provenance.
- NP616757.RAGtq_fcw6TIIWozo-xJNZPiYjVkAf-PtoTkroAwE8Qt4130_assertion SIO_000772 18925516 NP616757.RAGtq_fcw6TIIWozo-xJNZPiYjVkAf-PtoTkroAwE8Qt4130_provenance.
- NP616757.RAGtq_fcw6TIIWozo-xJNZPiYjVkAf-PtoTkroAwE8Qt4130_assertion wasDerivedFrom befree-20140225 NP616757.RAGtq_fcw6TIIWozo-xJNZPiYjVkAf-PtoTkroAwE8Qt4130_provenance.
- NP616757.RAGtq_fcw6TIIWozo-xJNZPiYjVkAf-PtoTkroAwE8Qt4130_assertion wasGeneratedBy ECO_0000203 NP616757.RAGtq_fcw6TIIWozo-xJNZPiYjVkAf-PtoTkroAwE8Qt4130_provenance.