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- source_evidence_literature type ECO_0000212 NP648598.RAAbvhwXV2V6Ri19C6iDU3-UTUNJ9N4f52fJTMUPcRha4130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP648598.RAAbvhwXV2V6Ri19C6iDU3-UTUNJ9N4f52fJTMUPcRha4130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP648598.RAAbvhwXV2V6Ri19C6iDU3-UTUNJ9N4f52fJTMUPcRha4130_provenance.
- NP648598.RAAbvhwXV2V6Ri19C6iDU3-UTUNJ9N4f52fJTMUPcRha4130_assertion description "[Complete or partial gene deletions were identified in seven cases for hMSH2 (5.7% of mutation-negative HNPCC; 4.3% of all HNPCC), no cases for hMLH1 and six cases for APC (25% of mutation negative FAP; 8% of all FAP).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP648598.RAAbvhwXV2V6Ri19C6iDU3-UTUNJ9N4f52fJTMUPcRha4130_provenance.
- NP648598.RAAbvhwXV2V6Ri19C6iDU3-UTUNJ9N4f52fJTMUPcRha4130_assertion evidence source_evidence_literature NP648598.RAAbvhwXV2V6Ri19C6iDU3-UTUNJ9N4f52fJTMUPcRha4130_provenance.
- NP648598.RAAbvhwXV2V6Ri19C6iDU3-UTUNJ9N4f52fJTMUPcRha4130_assertion SIO_000772 15475941 NP648598.RAAbvhwXV2V6Ri19C6iDU3-UTUNJ9N4f52fJTMUPcRha4130_provenance.
- NP648598.RAAbvhwXV2V6Ri19C6iDU3-UTUNJ9N4f52fJTMUPcRha4130_assertion wasDerivedFrom befree-20150227 NP648598.RAAbvhwXV2V6Ri19C6iDU3-UTUNJ9N4f52fJTMUPcRha4130_provenance.
- NP648598.RAAbvhwXV2V6Ri19C6iDU3-UTUNJ9N4f52fJTMUPcRha4130_assertion wasGeneratedBy ECO_0000203 NP648598.RAAbvhwXV2V6Ri19C6iDU3-UTUNJ9N4f52fJTMUPcRha4130_provenance.
- befree-20150227 importedOn "2015-02-27" NP648598.RAAbvhwXV2V6Ri19C6iDU3-UTUNJ9N4f52fJTMUPcRha4130_provenance.