Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP196647.RAqoBL4gMtCXtZZjjD2hAR0OiQWVAdzsJGT8JiEZ2kj-Q130_assertion> ?p ?o ?g. }
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- NP196647.RAqoBL4gMtCXtZZjjD2hAR0OiQWVAdzsJGT8JiEZ2kj-Q130_assertion type Assertion NP196647.RAqoBL4gMtCXtZZjjD2hAR0OiQWVAdzsJGT8JiEZ2kj-Q130_head.
- NP196647.RAqoBL4gMtCXtZZjjD2hAR0OiQWVAdzsJGT8JiEZ2kj-Q130_assertion wasGeneratedBy ECO_0000203 NP196647.RAqoBL4gMtCXtZZjjD2hAR0OiQWVAdzsJGT8JiEZ2kj-Q130_provenance.
- NP196647.RAqoBL4gMtCXtZZjjD2hAR0OiQWVAdzsJGT8JiEZ2kj-Q130_assertion wasDerivedFrom lhgdn-20090331 NP196647.RAqoBL4gMtCXtZZjjD2hAR0OiQWVAdzsJGT8JiEZ2kj-Q130_provenance.
- NP196647.RAqoBL4gMtCXtZZjjD2hAR0OiQWVAdzsJGT8JiEZ2kj-Q130_assertion SIO_000772 15146389 NP196647.RAqoBL4gMtCXtZZjjD2hAR0OiQWVAdzsJGT8JiEZ2kj-Q130_provenance.
- NP196647.RAqoBL4gMtCXtZZjjD2hAR0OiQWVAdzsJGT8JiEZ2kj-Q130_assertion evidence source_evidence_literature NP196647.RAqoBL4gMtCXtZZjjD2hAR0OiQWVAdzsJGT8JiEZ2kj-Q130_provenance.
- NP196647.RAqoBL4gMtCXtZZjjD2hAR0OiQWVAdzsJGT8JiEZ2kj-Q130_assertion description "[Missense Mutation in HOXD10 is associated with congenital vertical talus and Charcot-Marie-Tooth disease]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP196647.RAqoBL4gMtCXtZZjjD2hAR0OiQWVAdzsJGT8JiEZ2kj-Q130_provenance.