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- NP718775.RAv0irbKlFcWBGGk6zAl3aZ2l9wi6VG5_FnBfNqNlrua4130_assertion type Assertion NP718775.RAv0irbKlFcWBGGk6zAl3aZ2l9wi6VG5_FnBfNqNlrua4130_head.
- NP718775.RAv0irbKlFcWBGGk6zAl3aZ2l9wi6VG5_FnBfNqNlrua4130_assertion description "[A novel COL1A1 mutation in infantile cortical hyperostosis (Caffey disease) expands the spectrum of collagen-related disorders.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP718775.RAv0irbKlFcWBGGk6zAl3aZ2l9wi6VG5_FnBfNqNlrua4130_provenance.
- NP718775.RAv0irbKlFcWBGGk6zAl3aZ2l9wi6VG5_FnBfNqNlrua4130_assertion evidence source_evidence_literature NP718775.RAv0irbKlFcWBGGk6zAl3aZ2l9wi6VG5_FnBfNqNlrua4130_provenance.
- NP718775.RAv0irbKlFcWBGGk6zAl3aZ2l9wi6VG5_FnBfNqNlrua4130_assertion SIO_000772 15864348 NP718775.RAv0irbKlFcWBGGk6zAl3aZ2l9wi6VG5_FnBfNqNlrua4130_provenance.
- NP718775.RAv0irbKlFcWBGGk6zAl3aZ2l9wi6VG5_FnBfNqNlrua4130_assertion wasDerivedFrom befree-20140225 NP718775.RAv0irbKlFcWBGGk6zAl3aZ2l9wi6VG5_FnBfNqNlrua4130_provenance.
- NP718775.RAv0irbKlFcWBGGk6zAl3aZ2l9wi6VG5_FnBfNqNlrua4130_assertion wasGeneratedBy ECO_0000203 NP718775.RAv0irbKlFcWBGGk6zAl3aZ2l9wi6VG5_FnBfNqNlrua4130_provenance.