Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP694045.RAPIGXBBtacFf46m_fclgeMg-YqNAVAVhZ7zXW8q9_TiA130_assertion> ?p ?o ?g. }
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- NP694045.RAPIGXBBtacFf46m_fclgeMg-YqNAVAVhZ7zXW8q9_TiA130_assertion type Assertion NP694045.RAPIGXBBtacFf46m_fclgeMg-YqNAVAVhZ7zXW8q9_TiA130_head.
- NP694045.RAPIGXBBtacFf46m_fclgeMg-YqNAVAVhZ7zXW8q9_TiA130_assertion description "[The present study has shown high prevalence of p16INK4A mutations in Slovenian population of familial melanoma patients (37%) and an absence of p14ARF or CDK4 mutations.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP694045.RAPIGXBBtacFf46m_fclgeMg-YqNAVAVhZ7zXW8q9_TiA130_provenance.
- NP694045.RAPIGXBBtacFf46m_fclgeMg-YqNAVAVhZ7zXW8q9_TiA130_assertion evidence source_evidence_literature NP694045.RAPIGXBBtacFf46m_fclgeMg-YqNAVAVhZ7zXW8q9_TiA130_provenance.
- NP694045.RAPIGXBBtacFf46m_fclgeMg-YqNAVAVhZ7zXW8q9_TiA130_assertion SIO_000772 18803811 NP694045.RAPIGXBBtacFf46m_fclgeMg-YqNAVAVhZ7zXW8q9_TiA130_provenance.
- NP694045.RAPIGXBBtacFf46m_fclgeMg-YqNAVAVhZ7zXW8q9_TiA130_assertion wasDerivedFrom befree-2016 NP694045.RAPIGXBBtacFf46m_fclgeMg-YqNAVAVhZ7zXW8q9_TiA130_provenance.
- NP694045.RAPIGXBBtacFf46m_fclgeMg-YqNAVAVhZ7zXW8q9_TiA130_assertion wasGeneratedBy ECO_0000203 NP694045.RAPIGXBBtacFf46m_fclgeMg-YqNAVAVhZ7zXW8q9_TiA130_provenance.