Matches in Nanopublications for { <http://rdf.disgenet.org/nanopublications.trig#NP692546.RAP2w41eAyFxTAgRzfsB7SzNh5mtshxrUPusq7hNj4E7Q130_assertion> ?p ?o ?g. }
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- NP692546.RAP2w41eAyFxTAgRzfsB7SzNh5mtshxrUPusq7hNj4E7Q130_assertion type Assertion NP692546.RAP2w41eAyFxTAgRzfsB7SzNh5mtshxrUPusq7hNj4E7Q130_head.
- NP692546.RAP2w41eAyFxTAgRzfsB7SzNh5mtshxrUPusq7hNj4E7Q130_assertion description "[MYH9-related disorders are rare causes of chronic kidney disease (CKD) presenting as chronic glomerulonephritis and derive from mutations of the MYH9 gene, which encodes for the nonmuscle myosin heavy chain IIA.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP692546.RAP2w41eAyFxTAgRzfsB7SzNh5mtshxrUPusq7hNj4E7Q130_provenance.
- NP692546.RAP2w41eAyFxTAgRzfsB7SzNh5mtshxrUPusq7hNj4E7Q130_assertion evidence source_evidence_literature NP692546.RAP2w41eAyFxTAgRzfsB7SzNh5mtshxrUPusq7hNj4E7Q130_provenance.
- NP692546.RAP2w41eAyFxTAgRzfsB7SzNh5mtshxrUPusq7hNj4E7Q130_assertion SIO_000772 19726116 NP692546.RAP2w41eAyFxTAgRzfsB7SzNh5mtshxrUPusq7hNj4E7Q130_provenance.
- NP692546.RAP2w41eAyFxTAgRzfsB7SzNh5mtshxrUPusq7hNj4E7Q130_assertion wasDerivedFrom befree-20140225 NP692546.RAP2w41eAyFxTAgRzfsB7SzNh5mtshxrUPusq7hNj4E7Q130_provenance.
- NP692546.RAP2w41eAyFxTAgRzfsB7SzNh5mtshxrUPusq7hNj4E7Q130_assertion wasGeneratedBy ECO_0000203 NP692546.RAP2w41eAyFxTAgRzfsB7SzNh5mtshxrUPusq7hNj4E7Q130_provenance.