Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP1024909.RAJZTswFPDjz8xK5NqGm50ob0l0iyT2MX6FXRXsxXIqTg130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP1024909.RAJZTswFPDjz8xK5NqGm50ob0l0iyT2MX6FXRXsxXIqTg130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP1024909.RAJZTswFPDjz8xK5NqGm50ob0l0iyT2MX6FXRXsxXIqTg130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP1024909.RAJZTswFPDjz8xK5NqGm50ob0l0iyT2MX6FXRXsxXIqTg130_provenance.
- NP1024909.RAJZTswFPDjz8xK5NqGm50ob0l0iyT2MX6FXRXsxXIqTg130_assertion description "[The results support previous data indicating that mutations that are predicted to abolish barttin expression are associated with a severe phenotype and early onset renal failure.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1024909.RAJZTswFPDjz8xK5NqGm50ob0l0iyT2MX6FXRXsxXIqTg130_provenance.
- NP1024909.RAJZTswFPDjz8xK5NqGm50ob0l0iyT2MX6FXRXsxXIqTg130_assertion evidence source_evidence_literature NP1024909.RAJZTswFPDjz8xK5NqGm50ob0l0iyT2MX6FXRXsxXIqTg130_provenance.
- NP1024909.RAJZTswFPDjz8xK5NqGm50ob0l0iyT2MX6FXRXsxXIqTg130_assertion SIO_000772 23110775 NP1024909.RAJZTswFPDjz8xK5NqGm50ob0l0iyT2MX6FXRXsxXIqTg130_provenance.
- NP1024909.RAJZTswFPDjz8xK5NqGm50ob0l0iyT2MX6FXRXsxXIqTg130_assertion wasDerivedFrom befree-2016 NP1024909.RAJZTswFPDjz8xK5NqGm50ob0l0iyT2MX6FXRXsxXIqTg130_provenance.
- NP1024909.RAJZTswFPDjz8xK5NqGm50ob0l0iyT2MX6FXRXsxXIqTg130_assertion wasGeneratedBy ECO_0000203 NP1024909.RAJZTswFPDjz8xK5NqGm50ob0l0iyT2MX6FXRXsxXIqTg130_provenance.
- befree-2016 importedOn "2016-02-19" NP1024909.RAJZTswFPDjz8xK5NqGm50ob0l0iyT2MX6FXRXsxXIqTg130_provenance.