Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP939260.RAgrjqV7Ev5oBl6eH1UryTYlF3lAmX8rHlfTChVFSugwI130_assertion> ?p ?o ?g. }
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- NP939260.RAgrjqV7Ev5oBl6eH1UryTYlF3lAmX8rHlfTChVFSugwI130_assertion type Assertion NP939260.RAgrjqV7Ev5oBl6eH1UryTYlF3lAmX8rHlfTChVFSugwI130_head.
- NP939260.RAgrjqV7Ev5oBl6eH1UryTYlF3lAmX8rHlfTChVFSugwI130_assertion description "[Mutations in inverted formin, FH2, and WH2 domain containing (INF2) are common causes of dominant focal segmental glomerulosclerosis.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP939260.RAgrjqV7Ev5oBl6eH1UryTYlF3lAmX8rHlfTChVFSugwI130_provenance.
- NP939260.RAgrjqV7Ev5oBl6eH1UryTYlF3lAmX8rHlfTChVFSugwI130_assertion evidence source_evidence_literature NP939260.RAgrjqV7Ev5oBl6eH1UryTYlF3lAmX8rHlfTChVFSugwI130_provenance.
- NP939260.RAgrjqV7Ev5oBl6eH1UryTYlF3lAmX8rHlfTChVFSugwI130_assertion SIO_000772 22961558 NP939260.RAgrjqV7Ev5oBl6eH1UryTYlF3lAmX8rHlfTChVFSugwI130_provenance.
- NP939260.RAgrjqV7Ev5oBl6eH1UryTYlF3lAmX8rHlfTChVFSugwI130_assertion wasDerivedFrom befree-20150227 NP939260.RAgrjqV7Ev5oBl6eH1UryTYlF3lAmX8rHlfTChVFSugwI130_provenance.
- NP939260.RAgrjqV7Ev5oBl6eH1UryTYlF3lAmX8rHlfTChVFSugwI130_assertion wasGeneratedBy ECO_0000203 NP939260.RAgrjqV7Ev5oBl6eH1UryTYlF3lAmX8rHlfTChVFSugwI130_provenance.