Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP343278.RASHnTX1yZ0CLUK0mvMbLSka6SdeN0Qvi4lx6fUCEZmME130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP343278.RASHnTX1yZ0CLUK0mvMbLSka6SdeN0Qvi4lx6fUCEZmME130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP343278.RASHnTX1yZ0CLUK0mvMbLSka6SdeN0Qvi4lx6fUCEZmME130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP343278.RASHnTX1yZ0CLUK0mvMbLSka6SdeN0Qvi4lx6fUCEZmME130_provenance.
- NP343278.RASHnTX1yZ0CLUK0mvMbLSka6SdeN0Qvi4lx6fUCEZmME130_assertion description "[PHEX, a phosphate-regulating gene with homologies to endopeptidases on the X chromosome, is mutated in X-linked hypophosphatemia (XLH) in humans and mice (Hyp).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP343278.RASHnTX1yZ0CLUK0mvMbLSka6SdeN0Qvi4lx6fUCEZmME130_provenance.
- NP343278.RASHnTX1yZ0CLUK0mvMbLSka6SdeN0Qvi4lx6fUCEZmME130_assertion evidence source_evidence_literature NP343278.RASHnTX1yZ0CLUK0mvMbLSka6SdeN0Qvi4lx6fUCEZmME130_provenance.
- NP343278.RASHnTX1yZ0CLUK0mvMbLSka6SdeN0Qvi4lx6fUCEZmME130_assertion SIO_000772 11811562 NP343278.RASHnTX1yZ0CLUK0mvMbLSka6SdeN0Qvi4lx6fUCEZmME130_provenance.
- NP343278.RASHnTX1yZ0CLUK0mvMbLSka6SdeN0Qvi4lx6fUCEZmME130_assertion wasDerivedFrom befree-2016 NP343278.RASHnTX1yZ0CLUK0mvMbLSka6SdeN0Qvi4lx6fUCEZmME130_provenance.
- NP343278.RASHnTX1yZ0CLUK0mvMbLSka6SdeN0Qvi4lx6fUCEZmME130_assertion wasGeneratedBy ECO_0000203 NP343278.RASHnTX1yZ0CLUK0mvMbLSka6SdeN0Qvi4lx6fUCEZmME130_provenance.
- befree-2016 importedOn "2016-02-19" NP343278.RASHnTX1yZ0CLUK0mvMbLSka6SdeN0Qvi4lx6fUCEZmME130_provenance.