Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP91280.RAoxtsqQiInm7NgRSPN6bP3tz9u3NeXO_9y_SMVNNP1NM130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP91280.RAoxtsqQiInm7NgRSPN6bP3tz9u3NeXO_9y_SMVNNP1NM130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP91280.RAoxtsqQiInm7NgRSPN6bP3tz9u3NeXO_9y_SMVNNP1NM130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP91280.RAoxtsqQiInm7NgRSPN6bP3tz9u3NeXO_9y_SMVNNP1NM130_provenance.
- NP91280.RAoxtsqQiInm7NgRSPN6bP3tz9u3NeXO_9y_SMVNNP1NM130_assertion description "[ The results demonstrate that NPHS2 mutations are also present in Chinese sporadic SRNS. Our investigation supports the necessity of searching for mutations in NPHS2 in Chinese children with sporadic SRNS.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP91280.RAoxtsqQiInm7NgRSPN6bP3tz9u3NeXO_9y_SMVNNP1NM130_provenance.
- NP91280.RAoxtsqQiInm7NgRSPN6bP3tz9u3NeXO_9y_SMVNNP1NM130_assertion evidence source_evidence_literature NP91280.RAoxtsqQiInm7NgRSPN6bP3tz9u3NeXO_9y_SMVNNP1NM130_provenance.
- NP91280.RAoxtsqQiInm7NgRSPN6bP3tz9u3NeXO_9y_SMVNNP1NM130_assertion SIO_000772 15769810 NP91280.RAoxtsqQiInm7NgRSPN6bP3tz9u3NeXO_9y_SMVNNP1NM130_provenance.
- NP91280.RAoxtsqQiInm7NgRSPN6bP3tz9u3NeXO_9y_SMVNNP1NM130_assertion wasDerivedFrom gad-20150221 NP91280.RAoxtsqQiInm7NgRSPN6bP3tz9u3NeXO_9y_SMVNNP1NM130_provenance.
- NP91280.RAoxtsqQiInm7NgRSPN6bP3tz9u3NeXO_9y_SMVNNP1NM130_assertion wasGeneratedBy ECO_0000203 NP91280.RAoxtsqQiInm7NgRSPN6bP3tz9u3NeXO_9y_SMVNNP1NM130_provenance.
- gad-20150221 importedOn "2015-02-21" NP91280.RAoxtsqQiInm7NgRSPN6bP3tz9u3NeXO_9y_SMVNNP1NM130_provenance.