Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP783697.RAtG70kIbjT7QlRwxSLDWeb3nHnMjsSjvfzRTrFSo8A0g130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP783697.RAtG70kIbjT7QlRwxSLDWeb3nHnMjsSjvfzRTrFSo8A0g130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP783697.RAtG70kIbjT7QlRwxSLDWeb3nHnMjsSjvfzRTrFSo8A0g130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP783697.RAtG70kIbjT7QlRwxSLDWeb3nHnMjsSjvfzRTrFSo8A0g130_provenance.
- NP783697.RAtG70kIbjT7QlRwxSLDWeb3nHnMjsSjvfzRTrFSo8A0g130_assertion description "[Familial forms of FSGS do not recur, but the discovery of numerous patients with sporadic FSGS and mutations of podocin (NPHS2, that is actually an inherited disease) who received a renal graft require a re-evaluation of the problem.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP783697.RAtG70kIbjT7QlRwxSLDWeb3nHnMjsSjvfzRTrFSo8A0g130_provenance.
- NP783697.RAtG70kIbjT7QlRwxSLDWeb3nHnMjsSjvfzRTrFSo8A0g130_assertion evidence source_evidence_literature NP783697.RAtG70kIbjT7QlRwxSLDWeb3nHnMjsSjvfzRTrFSo8A0g130_provenance.
- NP783697.RAtG70kIbjT7QlRwxSLDWeb3nHnMjsSjvfzRTrFSo8A0g130_assertion SIO_000772 12776285 NP783697.RAtG70kIbjT7QlRwxSLDWeb3nHnMjsSjvfzRTrFSo8A0g130_provenance.
- NP783697.RAtG70kIbjT7QlRwxSLDWeb3nHnMjsSjvfzRTrFSo8A0g130_assertion wasDerivedFrom befree-20150227 NP783697.RAtG70kIbjT7QlRwxSLDWeb3nHnMjsSjvfzRTrFSo8A0g130_provenance.
- NP783697.RAtG70kIbjT7QlRwxSLDWeb3nHnMjsSjvfzRTrFSo8A0g130_assertion wasGeneratedBy ECO_0000203 NP783697.RAtG70kIbjT7QlRwxSLDWeb3nHnMjsSjvfzRTrFSo8A0g130_provenance.
- befree-20150227 importedOn "2015-02-27" NP783697.RAtG70kIbjT7QlRwxSLDWeb3nHnMjsSjvfzRTrFSo8A0g130_provenance.