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- NP294791.RAHSGMkmogiv8ybmgF-2LEPSd-U2UGSrP2f-3KngBk3dA130_assertion type Assertion NP294791.RAHSGMkmogiv8ybmgF-2LEPSd-U2UGSrP2f-3KngBk3dA130_head.
- NP294791.RAHSGMkmogiv8ybmgF-2LEPSd-U2UGSrP2f-3KngBk3dA130_assertion description "[Familial form of hirschsprung disease: nucleotide sequence studies reveal point mutations in the RET proto-oncogene in two of six families but not in other candidate genes.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP294791.RAHSGMkmogiv8ybmgF-2LEPSd-U2UGSrP2f-3KngBk3dA130_provenance.
- NP294791.RAHSGMkmogiv8ybmgF-2LEPSd-U2UGSrP2f-3KngBk3dA130_assertion evidence source_evidence_literature NP294791.RAHSGMkmogiv8ybmgF-2LEPSd-U2UGSrP2f-3KngBk3dA130_provenance.
- NP294791.RAHSGMkmogiv8ybmgF-2LEPSd-U2UGSrP2f-3KngBk3dA130_assertion SIO_000772 10982477 NP294791.RAHSGMkmogiv8ybmgF-2LEPSd-U2UGSrP2f-3KngBk3dA130_provenance.
- NP294791.RAHSGMkmogiv8ybmgF-2LEPSd-U2UGSrP2f-3KngBk3dA130_assertion wasDerivedFrom befree-2016 NP294791.RAHSGMkmogiv8ybmgF-2LEPSd-U2UGSrP2f-3KngBk3dA130_provenance.
- NP294791.RAHSGMkmogiv8ybmgF-2LEPSd-U2UGSrP2f-3KngBk3dA130_assertion wasGeneratedBy ECO_0000203 NP294791.RAHSGMkmogiv8ybmgF-2LEPSd-U2UGSrP2f-3KngBk3dA130_provenance.