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- source_evidence_literature type ECO_0000212 NP694045.RAPIGXBBtacFf46m_fclgeMg-YqNAVAVhZ7zXW8q9_TiA130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP694045.RAPIGXBBtacFf46m_fclgeMg-YqNAVAVhZ7zXW8q9_TiA130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP694045.RAPIGXBBtacFf46m_fclgeMg-YqNAVAVhZ7zXW8q9_TiA130_provenance.
- 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.
- befree-2016 importedOn "2016-02-19" NP694045.RAPIGXBBtacFf46m_fclgeMg-YqNAVAVhZ7zXW8q9_TiA130_provenance.