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- source_evidence_literature type ECO_0000212 NP587266.RAfIePtSPEnkXmc6vPZXtMVyD62JQu9XWwNaKonTElr6U130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP587266.RAfIePtSPEnkXmc6vPZXtMVyD62JQu9XWwNaKonTElr6U130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP587266.RAfIePtSPEnkXmc6vPZXtMVyD62JQu9XWwNaKonTElr6U130_provenance.
- befree-2016 importedOn "2016-02-19" NP587266.RAfIePtSPEnkXmc6vPZXtMVyD62JQu9XWwNaKonTElr6U130_provenance.
- NP587266.RAfIePtSPEnkXmc6vPZXtMVyD62JQu9XWwNaKonTElr6U130_assertion wasGeneratedBy ECO_0000203 NP587266.RAfIePtSPEnkXmc6vPZXtMVyD62JQu9XWwNaKonTElr6U130_provenance.
- NP587266.RAfIePtSPEnkXmc6vPZXtMVyD62JQu9XWwNaKonTElr6U130_assertion wasDerivedFrom befree-2016 NP587266.RAfIePtSPEnkXmc6vPZXtMVyD62JQu9XWwNaKonTElr6U130_provenance.
- NP587266.RAfIePtSPEnkXmc6vPZXtMVyD62JQu9XWwNaKonTElr6U130_assertion SIO_000772 17204026 NP587266.RAfIePtSPEnkXmc6vPZXtMVyD62JQu9XWwNaKonTElr6U130_provenance.
- NP587266.RAfIePtSPEnkXmc6vPZXtMVyD62JQu9XWwNaKonTElr6U130_assertion evidence source_evidence_literature NP587266.RAfIePtSPEnkXmc6vPZXtMVyD62JQu9XWwNaKonTElr6U130_provenance.
- NP587266.RAfIePtSPEnkXmc6vPZXtMVyD62JQu9XWwNaKonTElr6U130_assertion description "[In this review the morphological correlates of five molecular subtypes are outlined: Type 1 (CIMP-high/MSI-H/BRAF mutation), Type 2 (CIMP-high/MSI-L or MSS/BRAF mutation), Type 3 (CIMP-low/MSS or MSI-L/KRAS mutation), Type 4 (CIMP-neg/MSS) and Type 5 or Lynch syndrome (CIMP-neg/MSI-H).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP587266.RAfIePtSPEnkXmc6vPZXtMVyD62JQu9XWwNaKonTElr6U130_provenance.