Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP857102.RA4hwjxmrF2wAMNCZfi-Z9FjxFQAKKlFaIuGBKJJkaQeg130_assertion> ?p ?o ?g. }
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- NP857102.RA4hwjxmrF2wAMNCZfi-Z9FjxFQAKKlFaIuGBKJJkaQeg130_assertion type Assertion NP857102.RA4hwjxmrF2wAMNCZfi-Z9FjxFQAKKlFaIuGBKJJkaQeg130_head.
- NP857102.RA4hwjxmrF2wAMNCZfi-Z9FjxFQAKKlFaIuGBKJJkaQeg130_assertion description "[The most frequent p63 mutation syndrome is the EEC syndrome, characterized by ectrodactyly, ectodermal dysplasia and cleft lip/palate.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP857102.RA4hwjxmrF2wAMNCZfi-Z9FjxFQAKKlFaIuGBKJJkaQeg130_provenance.
- NP857102.RA4hwjxmrF2wAMNCZfi-Z9FjxFQAKKlFaIuGBKJJkaQeg130_assertion evidence source_evidence_literature NP857102.RA4hwjxmrF2wAMNCZfi-Z9FjxFQAKKlFaIuGBKJJkaQeg130_provenance.
- NP857102.RA4hwjxmrF2wAMNCZfi-Z9FjxFQAKKlFaIuGBKJJkaQeg130_assertion SIO_000772 23407076 NP857102.RA4hwjxmrF2wAMNCZfi-Z9FjxFQAKKlFaIuGBKJJkaQeg130_provenance.
- NP857102.RA4hwjxmrF2wAMNCZfi-Z9FjxFQAKKlFaIuGBKJJkaQeg130_assertion wasDerivedFrom befree-20150227 NP857102.RA4hwjxmrF2wAMNCZfi-Z9FjxFQAKKlFaIuGBKJJkaQeg130_provenance.
- NP857102.RA4hwjxmrF2wAMNCZfi-Z9FjxFQAKKlFaIuGBKJJkaQeg130_assertion wasGeneratedBy ECO_0000203 NP857102.RA4hwjxmrF2wAMNCZfi-Z9FjxFQAKKlFaIuGBKJJkaQeg130_provenance.