Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP305675.RAyLpFP1NEP-QqLvsdTzBPgpcYLdv5LLfZQYK3npSAkUM130_assertion> ?p ?o ?g. }
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- NP305675.RAyLpFP1NEP-QqLvsdTzBPgpcYLdv5LLfZQYK3npSAkUM130_assertion type Assertion NP305675.RAyLpFP1NEP-QqLvsdTzBPgpcYLdv5LLfZQYK3npSAkUM130_head.
- NP305675.RAyLpFP1NEP-QqLvsdTzBPgpcYLdv5LLfZQYK3npSAkUM130_assertion wasGeneratedBy ECO_0000203 NP305675.RAyLpFP1NEP-QqLvsdTzBPgpcYLdv5LLfZQYK3npSAkUM130_provenance.
- NP305675.RAyLpFP1NEP-QqLvsdTzBPgpcYLdv5LLfZQYK3npSAkUM130_assertion wasDerivedFrom befree-2016 NP305675.RAyLpFP1NEP-QqLvsdTzBPgpcYLdv5LLfZQYK3npSAkUM130_provenance.
- NP305675.RAyLpFP1NEP-QqLvsdTzBPgpcYLdv5LLfZQYK3npSAkUM130_assertion SIO_000772 11159940 NP305675.RAyLpFP1NEP-QqLvsdTzBPgpcYLdv5LLfZQYK3npSAkUM130_provenance.
- NP305675.RAyLpFP1NEP-QqLvsdTzBPgpcYLdv5LLfZQYK3npSAkUM130_assertion evidence source_evidence_literature NP305675.RAyLpFP1NEP-QqLvsdTzBPgpcYLdv5LLfZQYK3npSAkUM130_provenance.
- NP305675.RAyLpFP1NEP-QqLvsdTzBPgpcYLdv5LLfZQYK3npSAkUM130_assertion description "[Hay-Wells syndrome is caused by heterozygous missense mutations in the SAM domain of p63.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP305675.RAyLpFP1NEP-QqLvsdTzBPgpcYLdv5LLfZQYK3npSAkUM130_provenance.