Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP17434.RAtRBwvfpmfxXU_6hgsHw2PaJvR51n4sCdRuoZ5YZ45lU130_provenance>. }
Showing items 1 to 9 of
9
with 100 items per page.
- source_evidence_curated type ECO_0000205 NP17434.RAtRBwvfpmfxXU_6hgsHw2PaJvR51n4sCdRuoZ5YZ45lU130_provenance.
- source_evidence_curated label "DisGeNET evidence - CURATED" NP17434.RAtRBwvfpmfxXU_6hgsHw2PaJvR51n4sCdRuoZ5YZ45lU130_provenance.
- source_evidence_curated comment "Gene-disease associations manually curated." NP17434.RAtRBwvfpmfxXU_6hgsHw2PaJvR51n4sCdRuoZ5YZ45lU130_provenance.
- ctd_human-20150221 importedOn "2015-02-21" NP17434.RAtRBwvfpmfxXU_6hgsHw2PaJvR51n4sCdRuoZ5YZ45lU130_provenance.
- NP17434.RAtRBwvfpmfxXU_6hgsHw2PaJvR51n4sCdRuoZ5YZ45lU130_assertion wasGeneratedBy ECO_0000218 NP17434.RAtRBwvfpmfxXU_6hgsHw2PaJvR51n4sCdRuoZ5YZ45lU130_provenance.
- NP17434.RAtRBwvfpmfxXU_6hgsHw2PaJvR51n4sCdRuoZ5YZ45lU130_assertion wasDerivedFrom ctd_human-20150221 NP17434.RAtRBwvfpmfxXU_6hgsHw2PaJvR51n4sCdRuoZ5YZ45lU130_provenance.
- NP17434.RAtRBwvfpmfxXU_6hgsHw2PaJvR51n4sCdRuoZ5YZ45lU130_assertion SIO_000772 15146389 NP17434.RAtRBwvfpmfxXU_6hgsHw2PaJvR51n4sCdRuoZ5YZ45lU130_provenance.
- NP17434.RAtRBwvfpmfxXU_6hgsHw2PaJvR51n4sCdRuoZ5YZ45lU130_assertion evidence source_evidence_curated NP17434.RAtRBwvfpmfxXU_6hgsHw2PaJvR51n4sCdRuoZ5YZ45lU130_provenance.
- NP17434.RAtRBwvfpmfxXU_6hgsHw2PaJvR51n4sCdRuoZ5YZ45lU130_assertion description "[A HOX gene mutation in a family with isolated congenital vertical talus and Charcot-Marie-Tooth disease.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP17434.RAtRBwvfpmfxXU_6hgsHw2PaJvR51n4sCdRuoZ5YZ45lU130_provenance.