Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP519704.RAEf0TYcTFHfg8O_3Z3zxO3jdKhW6yVtkp8dL9Qc5qHeE130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP519704.RAEf0TYcTFHfg8O_3Z3zxO3jdKhW6yVtkp8dL9Qc5qHeE130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP519704.RAEf0TYcTFHfg8O_3Z3zxO3jdKhW6yVtkp8dL9Qc5qHeE130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP519704.RAEf0TYcTFHfg8O_3Z3zxO3jdKhW6yVtkp8dL9Qc5qHeE130_provenance.
- 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.
- befree-2016 importedOn "2016-02-19" NP519704.RAEf0TYcTFHfg8O_3Z3zxO3jdKhW6yVtkp8dL9Qc5qHeE130_provenance.