Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP2137.RACXfhiniVye9lCeZxPCCjdyoPEB-fUMLmAnFcee1ULos130_assertion> ?p ?o ?g. }
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- NP2137.RACXfhiniVye9lCeZxPCCjdyoPEB-fUMLmAnFcee1ULos130_assertion type Assertion NP2137.RACXfhiniVye9lCeZxPCCjdyoPEB-fUMLmAnFcee1ULos130_head.
- NP2137.RACXfhiniVye9lCeZxPCCjdyoPEB-fUMLmAnFcee1ULos130_assertion wasGeneratedBy ECO_0000218 NP2137.RACXfhiniVye9lCeZxPCCjdyoPEB-fUMLmAnFcee1ULos130_provenance.
- NP2137.RACXfhiniVye9lCeZxPCCjdyoPEB-fUMLmAnFcee1ULos130_assertion wasDerivedFrom uniprot-20150221 NP2137.RACXfhiniVye9lCeZxPCCjdyoPEB-fUMLmAnFcee1ULos130_provenance.
- NP2137.RACXfhiniVye9lCeZxPCCjdyoPEB-fUMLmAnFcee1ULos130_assertion SIO_000772 15146389 NP2137.RACXfhiniVye9lCeZxPCCjdyoPEB-fUMLmAnFcee1ULos130_provenance.
- NP2137.RACXfhiniVye9lCeZxPCCjdyoPEB-fUMLmAnFcee1ULos130_assertion evidence source_evidence_curated NP2137.RACXfhiniVye9lCeZxPCCjdyoPEB-fUMLmAnFcee1ULos130_provenance.
- NP2137.RACXfhiniVye9lCeZxPCCjdyoPEB-fUMLmAnFcee1ULos130_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." NP2137.RACXfhiniVye9lCeZxPCCjdyoPEB-fUMLmAnFcee1ULos130_provenance.