Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP611813.RAS2xGtjnHLbDN1ai9ZSYnv5Mud6TdoTreNij8cepUBlQ130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP611813.RAS2xGtjnHLbDN1ai9ZSYnv5Mud6TdoTreNij8cepUBlQ130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP611813.RAS2xGtjnHLbDN1ai9ZSYnv5Mud6TdoTreNij8cepUBlQ130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP611813.RAS2xGtjnHLbDN1ai9ZSYnv5Mud6TdoTreNij8cepUBlQ130_provenance.
- NP611813.RAS2xGtjnHLbDN1ai9ZSYnv5Mud6TdoTreNij8cepUBlQ130_assertion description "[First, two thirds of nephrotic syndrome manifesting in the first year of life can be explained by mutations in 4 genes only (NPHS1, NPHS2, WT1, or LAMB2).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP611813.RAS2xGtjnHLbDN1ai9ZSYnv5Mud6TdoTreNij8cepUBlQ130_provenance.
- NP611813.RAS2xGtjnHLbDN1ai9ZSYnv5Mud6TdoTreNij8cepUBlQ130_assertion evidence source_evidence_literature NP611813.RAS2xGtjnHLbDN1ai9ZSYnv5Mud6TdoTreNij8cepUBlQ130_provenance.
- NP611813.RAS2xGtjnHLbDN1ai9ZSYnv5Mud6TdoTreNij8cepUBlQ130_assertion SIO_000772 17371932 NP611813.RAS2xGtjnHLbDN1ai9ZSYnv5Mud6TdoTreNij8cepUBlQ130_provenance.
- NP611813.RAS2xGtjnHLbDN1ai9ZSYnv5Mud6TdoTreNij8cepUBlQ130_assertion wasDerivedFrom befree-20140225 NP611813.RAS2xGtjnHLbDN1ai9ZSYnv5Mud6TdoTreNij8cepUBlQ130_provenance.
- NP611813.RAS2xGtjnHLbDN1ai9ZSYnv5Mud6TdoTreNij8cepUBlQ130_assertion wasGeneratedBy ECO_0000203 NP611813.RAS2xGtjnHLbDN1ai9ZSYnv5Mud6TdoTreNij8cepUBlQ130_provenance.
- befree-20140225 importedOn "2014-02-25" NP611813.RAS2xGtjnHLbDN1ai9ZSYnv5Mud6TdoTreNij8cepUBlQ130_provenance.