Matches in Nanopublications for { ?s ?p "[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."@en ?g. }
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- NP390846.RAAj9r9dyzXYWrsZJrNIeGO7qVvrslcniS270u1a_qOOA130_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." NP390846.RAAj9r9dyzXYWrsZJrNIeGO7qVvrslcniS270u1a_qOOA130_provenance.
- NP417662.RA9DodccQAXumBNoOvA_pmfBSa9mBSJlElYBsz4RNq2rM130_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." NP417662.RA9DodccQAXumBNoOvA_pmfBSa9mBSJlElYBsz4RNq2rM130_provenance.
- 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." provenance.
- NP390845.RAdyWLDJEiYOZax-nZRS2eCXsGX6ceIyIYrJodevUWh98130_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." NP390845.RAdyWLDJEiYOZax-nZRS2eCXsGX6ceIyIYrJodevUWh98130_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.