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- source_evidence_literature type ECO_0000212 NP283481.RADGCgvqArhzwuPjdgiWWejvj2InS_NuTYTwC615js1nI130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP283481.RADGCgvqArhzwuPjdgiWWejvj2InS_NuTYTwC615js1nI130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP283481.RADGCgvqArhzwuPjdgiWWejvj2InS_NuTYTwC615js1nI130_provenance.
- befree-2016 importedOn "2016-02-19" NP283481.RADGCgvqArhzwuPjdgiWWejvj2InS_NuTYTwC615js1nI130_provenance.
- NP283481.RADGCgvqArhzwuPjdgiWWejvj2InS_NuTYTwC615js1nI130_assertion wasGeneratedBy ECO_0000203 NP283481.RADGCgvqArhzwuPjdgiWWejvj2InS_NuTYTwC615js1nI130_provenance.
- NP283481.RADGCgvqArhzwuPjdgiWWejvj2InS_NuTYTwC615js1nI130_assertion wasDerivedFrom befree-2016 NP283481.RADGCgvqArhzwuPjdgiWWejvj2InS_NuTYTwC615js1nI130_provenance.
- NP283481.RADGCgvqArhzwuPjdgiWWejvj2InS_NuTYTwC615js1nI130_assertion SIO_000772 10805952 NP283481.RADGCgvqArhzwuPjdgiWWejvj2InS_NuTYTwC615js1nI130_provenance.
- NP283481.RADGCgvqArhzwuPjdgiWWejvj2InS_NuTYTwC615js1nI130_assertion evidence source_evidence_literature NP283481.RADGCgvqArhzwuPjdgiWWejvj2InS_NuTYTwC615js1nI130_provenance.
- NP283481.RADGCgvqArhzwuPjdgiWWejvj2InS_NuTYTwC615js1nI130_assertion description "[Discoveries in the 1990s of germ-line mutations, the most common of which are hMSH2 and hMLH1, have added enormous power to the diagnosis of Lynch syndrome.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP283481.RADGCgvqArhzwuPjdgiWWejvj2InS_NuTYTwC615js1nI130_provenance.