Matches in Nanopublications for { <http://rdf.disgenet.org/nanopublications.trig#NP555014.RAv37_JpyA1Ym-yCNUQxgZXgpraGHTvBapU60iVymWMR4130_assertion> ?p ?o ?g. }
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- NP555014.RAv37_JpyA1Ym-yCNUQxgZXgpraGHTvBapU60iVymWMR4130_assertion type Assertion NP555014.RAv37_JpyA1Ym-yCNUQxgZXgpraGHTvBapU60iVymWMR4130_head.
- NP555014.RAv37_JpyA1Ym-yCNUQxgZXgpraGHTvBapU60iVymWMR4130_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." NP555014.RAv37_JpyA1Ym-yCNUQxgZXgpraGHTvBapU60iVymWMR4130_provenance.
- NP555014.RAv37_JpyA1Ym-yCNUQxgZXgpraGHTvBapU60iVymWMR4130_assertion evidence source_evidence_literature NP555014.RAv37_JpyA1Ym-yCNUQxgZXgpraGHTvBapU60iVymWMR4130_provenance.
- NP555014.RAv37_JpyA1Ym-yCNUQxgZXgpraGHTvBapU60iVymWMR4130_assertion SIO_000772 18925516 NP555014.RAv37_JpyA1Ym-yCNUQxgZXgpraGHTvBapU60iVymWMR4130_provenance.
- NP555014.RAv37_JpyA1Ym-yCNUQxgZXgpraGHTvBapU60iVymWMR4130_assertion wasDerivedFrom befree-20140225 NP555014.RAv37_JpyA1Ym-yCNUQxgZXgpraGHTvBapU60iVymWMR4130_provenance.
- NP555014.RAv37_JpyA1Ym-yCNUQxgZXgpraGHTvBapU60iVymWMR4130_assertion wasGeneratedBy ECO_0000203 NP555014.RAv37_JpyA1Ym-yCNUQxgZXgpraGHTvBapU60iVymWMR4130_provenance.