Matches in Nanopublications for { <http://rdf.disgenet.org/nanopublications.trig#NP4165.RASlLJQVisnmKs4d41obREf9SOrhgMPtdaxPyEH2ZfRr4130_assertion> ?p ?o ?g. }
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- NP4165.RASlLJQVisnmKs4d41obREf9SOrhgMPtdaxPyEH2ZfRr4130_assertion type Assertion NP4165.RASlLJQVisnmKs4d41obREf9SOrhgMPtdaxPyEH2ZfRr4130_head.
- NP4165.RASlLJQVisnmKs4d41obREf9SOrhgMPtdaxPyEH2ZfRr4130_assertion wasGeneratedBy ECO_0000218 NP4165.RASlLJQVisnmKs4d41obREf9SOrhgMPtdaxPyEH2ZfRr4130_provenance.
- NP4165.RASlLJQVisnmKs4d41obREf9SOrhgMPtdaxPyEH2ZfRr4130_assertion wasDerivedFrom uniprot-20130724 NP4165.RASlLJQVisnmKs4d41obREf9SOrhgMPtdaxPyEH2ZfRr4130_provenance.
- NP4165.RASlLJQVisnmKs4d41obREf9SOrhgMPtdaxPyEH2ZfRr4130_assertion SIO_000772 8696335 NP4165.RASlLJQVisnmKs4d41obREf9SOrhgMPtdaxPyEH2ZfRr4130_provenance.
- NP4165.RASlLJQVisnmKs4d41obREf9SOrhgMPtdaxPyEH2ZfRr4130_assertion evidence source_evidence_curated NP4165.RASlLJQVisnmKs4d41obREf9SOrhgMPtdaxPyEH2ZfRr4130_provenance.
- NP4165.RASlLJQVisnmKs4d41obREf9SOrhgMPtdaxPyEH2ZfRr4130_assertion description "[We demonstrate that a mutation in the homeobox gene, MSX1, causes a common developmental anomaly, familial tooth agenesis.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP4165.RASlLJQVisnmKs4d41obREf9SOrhgMPtdaxPyEH2ZfRr4130_provenance.