Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP296376.RAtHJhbjaJk_b_3_Q2KgJpoJqDN7h5HeKlHq6S2EETWSo130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP296376.RAtHJhbjaJk_b_3_Q2KgJpoJqDN7h5HeKlHq6S2EETWSo130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP296376.RAtHJhbjaJk_b_3_Q2KgJpoJqDN7h5HeKlHq6S2EETWSo130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP296376.RAtHJhbjaJk_b_3_Q2KgJpoJqDN7h5HeKlHq6S2EETWSo130_provenance.
- NP296376.RAtHJhbjaJk_b_3_Q2KgJpoJqDN7h5HeKlHq6S2EETWSo130_assertion description "[Mutations in the p63 gene have recently been delineated as the molecular basis for some cases of the ectrodactyly, ectodermal dysplasia and cleft lip/palate (EEC) syndrome, an autosomal dominant disorder (MIM 129900).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP296376.RAtHJhbjaJk_b_3_Q2KgJpoJqDN7h5HeKlHq6S2EETWSo130_provenance.
- NP296376.RAtHJhbjaJk_b_3_Q2KgJpoJqDN7h5HeKlHq6S2EETWSo130_assertion evidence source_evidence_literature NP296376.RAtHJhbjaJk_b_3_Q2KgJpoJqDN7h5HeKlHq6S2EETWSo130_provenance.
- NP296376.RAtHJhbjaJk_b_3_Q2KgJpoJqDN7h5HeKlHq6S2EETWSo130_assertion SIO_000772 11012604 NP296376.RAtHJhbjaJk_b_3_Q2KgJpoJqDN7h5HeKlHq6S2EETWSo130_provenance.
- NP296376.RAtHJhbjaJk_b_3_Q2KgJpoJqDN7h5HeKlHq6S2EETWSo130_assertion wasDerivedFrom befree-2016 NP296376.RAtHJhbjaJk_b_3_Q2KgJpoJqDN7h5HeKlHq6S2EETWSo130_provenance.
- NP296376.RAtHJhbjaJk_b_3_Q2KgJpoJqDN7h5HeKlHq6S2EETWSo130_assertion wasGeneratedBy ECO_0000203 NP296376.RAtHJhbjaJk_b_3_Q2KgJpoJqDN7h5HeKlHq6S2EETWSo130_provenance.
- befree-2016 importedOn "2016-02-19" NP296376.RAtHJhbjaJk_b_3_Q2KgJpoJqDN7h5HeKlHq6S2EETWSo130_provenance.