Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP519704.RAEf0TYcTFHfg8O_3Z3zxO3jdKhW6yVtkp8dL9Qc5qHeE130_assertion> ?p ?o ?g. }
Showing items 1 to 6 of
6
with 100 items per page.
- NP519704.RAEf0TYcTFHfg8O_3Z3zxO3jdKhW6yVtkp8dL9Qc5qHeE130_assertion type Assertion NP519704.RAEf0TYcTFHfg8O_3Z3zxO3jdKhW6yVtkp8dL9Qc5qHeE130_head.
- NP519704.RAEf0TYcTFHfg8O_3Z3zxO3jdKhW6yVtkp8dL9Qc5qHeE130_assertion description "[ACTN4 mutations seem to account for approximately 4% of familial FSGS.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP519704.RAEf0TYcTFHfg8O_3Z3zxO3jdKhW6yVtkp8dL9Qc5qHeE130_provenance.
- NP519704.RAEf0TYcTFHfg8O_3Z3zxO3jdKhW6yVtkp8dL9Qc5qHeE130_assertion evidence source_evidence_literature NP519704.RAEf0TYcTFHfg8O_3Z3zxO3jdKhW6yVtkp8dL9Qc5qHeE130_provenance.
- NP519704.RAEf0TYcTFHfg8O_3Z3zxO3jdKhW6yVtkp8dL9Qc5qHeE130_assertion SIO_000772 16251236 NP519704.RAEf0TYcTFHfg8O_3Z3zxO3jdKhW6yVtkp8dL9Qc5qHeE130_provenance.
- NP519704.RAEf0TYcTFHfg8O_3Z3zxO3jdKhW6yVtkp8dL9Qc5qHeE130_assertion wasDerivedFrom befree-2016 NP519704.RAEf0TYcTFHfg8O_3Z3zxO3jdKhW6yVtkp8dL9Qc5qHeE130_provenance.
- NP519704.RAEf0TYcTFHfg8O_3Z3zxO3jdKhW6yVtkp8dL9Qc5qHeE130_assertion wasGeneratedBy ECO_0000203 NP519704.RAEf0TYcTFHfg8O_3Z3zxO3jdKhW6yVtkp8dL9Qc5qHeE130_provenance.