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- source_evidence_literature type ECO_0000212 NP54212.RAG6rA-YZMvsob6pM2Td-GrlS1WyPYghVRFmz_WwNaI7g130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP54212.RAG6rA-YZMvsob6pM2Td-GrlS1WyPYghVRFmz_WwNaI7g130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP54212.RAG6rA-YZMvsob6pM2Td-GrlS1WyPYghVRFmz_WwNaI7g130_provenance.
- NP54212.RAG6rA-YZMvsob6pM2Td-GrlS1WyPYghVRFmz_WwNaI7g130_assertion description "[In summary, biallelic germline mutations of MYH are unlikely to cause colorectal cancer in patients sharing clinical features with hereditary nonpolyposis colorectal cancer families without mismatch repair defect and therefore cannot fill the molecular diagnostic gap in this subgroup of Bethesda-positive patients.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP54212.RAG6rA-YZMvsob6pM2Td-GrlS1WyPYghVRFmz_WwNaI7g130_provenance.
- NP54212.RAG6rA-YZMvsob6pM2Td-GrlS1WyPYghVRFmz_WwNaI7g130_assertion evidence source_evidence_literature NP54212.RAG6rA-YZMvsob6pM2Td-GrlS1WyPYghVRFmz_WwNaI7g130_provenance.
- NP54212.RAG6rA-YZMvsob6pM2Td-GrlS1WyPYghVRFmz_WwNaI7g130_assertion SIO_000772 16645203 NP54212.RAG6rA-YZMvsob6pM2Td-GrlS1WyPYghVRFmz_WwNaI7g130_provenance.
- NP54212.RAG6rA-YZMvsob6pM2Td-GrlS1WyPYghVRFmz_WwNaI7g130_assertion wasDerivedFrom gad-20130706 NP54212.RAG6rA-YZMvsob6pM2Td-GrlS1WyPYghVRFmz_WwNaI7g130_provenance.
- NP54212.RAG6rA-YZMvsob6pM2Td-GrlS1WyPYghVRFmz_WwNaI7g130_assertion wasGeneratedBy ECO_0000203 NP54212.RAG6rA-YZMvsob6pM2Td-GrlS1WyPYghVRFmz_WwNaI7g130_provenance.
- gad-20130706 importedOn "2013-07-06" NP54212.RAG6rA-YZMvsob6pM2Td-GrlS1WyPYghVRFmz_WwNaI7g130_provenance.