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- NP417692.RAET6JCnMeILeISWUIRiHijJ7wHIdcXW4MbC5ts0rqFWU130_assertion type Assertion NP417692.RAET6JCnMeILeISWUIRiHijJ7wHIdcXW4MbC5ts0rqFWU130_head.
- NP417692.RAET6JCnMeILeISWUIRiHijJ7wHIdcXW4MbC5ts0rqFWU130_assertion wasGeneratedBy ECO_0000203 NP417692.RAET6JCnMeILeISWUIRiHijJ7wHIdcXW4MbC5ts0rqFWU130_provenance.
- NP417692.RAET6JCnMeILeISWUIRiHijJ7wHIdcXW4MbC5ts0rqFWU130_assertion wasDerivedFrom befree-20150227 NP417692.RAET6JCnMeILeISWUIRiHijJ7wHIdcXW4MbC5ts0rqFWU130_provenance.
- NP417692.RAET6JCnMeILeISWUIRiHijJ7wHIdcXW4MbC5ts0rqFWU130_assertion SIO_000772 12694189 NP417692.RAET6JCnMeILeISWUIRiHijJ7wHIdcXW4MbC5ts0rqFWU130_provenance.
- NP417692.RAET6JCnMeILeISWUIRiHijJ7wHIdcXW4MbC5ts0rqFWU130_assertion evidence source_evidence_literature NP417692.RAET6JCnMeILeISWUIRiHijJ7wHIdcXW4MbC5ts0rqFWU130_provenance.
- NP417692.RAET6JCnMeILeISWUIRiHijJ7wHIdcXW4MbC5ts0rqFWU130_assertion description "[Lack of fully functional galactokinase is one cause of the inherited disease galactosemia, the main clinical manifestation of which is early onset cataracts.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP417692.RAET6JCnMeILeISWUIRiHijJ7wHIdcXW4MbC5ts0rqFWU130_provenance.