Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP7837.RAO-tEVxRF3JZACwJq5qi__3_Jfdt3E5mQO80zCoG1vfo130_provenance>. }
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- source_evidence_curated type ECO_0000205 NP7837.RAO-tEVxRF3JZACwJq5qi__3_Jfdt3E5mQO80zCoG1vfo130_provenance.
- source_evidence_curated label "DisGeNET evidence - CURATED" NP7837.RAO-tEVxRF3JZACwJq5qi__3_Jfdt3E5mQO80zCoG1vfo130_provenance.
- source_evidence_curated comment "Gene-disease associations manually curated." NP7837.RAO-tEVxRF3JZACwJq5qi__3_Jfdt3E5mQO80zCoG1vfo130_provenance.
- uniprot-2016 importedOn "2016-01-25" NP7837.RAO-tEVxRF3JZACwJq5qi__3_Jfdt3E5mQO80zCoG1vfo130_provenance.
- NP7837.RAO-tEVxRF3JZACwJq5qi__3_Jfdt3E5mQO80zCoG1vfo130_assertion wasGeneratedBy ECO_0000218 NP7837.RAO-tEVxRF3JZACwJq5qi__3_Jfdt3E5mQO80zCoG1vfo130_provenance.
- NP7837.RAO-tEVxRF3JZACwJq5qi__3_Jfdt3E5mQO80zCoG1vfo130_assertion wasDerivedFrom uniprot-2016 NP7837.RAO-tEVxRF3JZACwJq5qi__3_Jfdt3E5mQO80zCoG1vfo130_provenance.
- NP7837.RAO-tEVxRF3JZACwJq5qi__3_Jfdt3E5mQO80zCoG1vfo130_assertion SIO_000772 24680727 NP7837.RAO-tEVxRF3JZACwJq5qi__3_Jfdt3E5mQO80zCoG1vfo130_provenance.
- NP7837.RAO-tEVxRF3JZACwJq5qi__3_Jfdt3E5mQO80zCoG1vfo130_assertion evidence source_evidence_curated NP7837.RAO-tEVxRF3JZACwJq5qi__3_Jfdt3E5mQO80zCoG1vfo130_provenance.
- NP7837.RAO-tEVxRF3JZACwJq5qi__3_Jfdt3E5mQO80zCoG1vfo130_assertion description "[A new missense mutation in FGF23 gene in a male with hyperostosis-hyperphosphatemia syndrome (HHS).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP7837.RAO-tEVxRF3JZACwJq5qi__3_Jfdt3E5mQO80zCoG1vfo130_provenance.