Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP417662.RA9DodccQAXumBNoOvA_pmfBSa9mBSJlElYBsz4RNq2rM130_assertion> ?p ?o ?g. }
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- NP417662.RA9DodccQAXumBNoOvA_pmfBSa9mBSJlElYBsz4RNq2rM130_assertion type Assertion NP417662.RA9DodccQAXumBNoOvA_pmfBSa9mBSJlElYBsz4RNq2rM130_head.
- NP417662.RA9DodccQAXumBNoOvA_pmfBSa9mBSJlElYBsz4RNq2rM130_assertion wasGeneratedBy ECO_0000203 NP417662.RA9DodccQAXumBNoOvA_pmfBSa9mBSJlElYBsz4RNq2rM130_provenance.
- NP417662.RA9DodccQAXumBNoOvA_pmfBSa9mBSJlElYBsz4RNq2rM130_assertion wasDerivedFrom befree-20150227 NP417662.RA9DodccQAXumBNoOvA_pmfBSa9mBSJlElYBsz4RNq2rM130_provenance.
- NP417662.RA9DodccQAXumBNoOvA_pmfBSa9mBSJlElYBsz4RNq2rM130_assertion SIO_000772 12694189 NP417662.RA9DodccQAXumBNoOvA_pmfBSa9mBSJlElYBsz4RNq2rM130_provenance.
- NP417662.RA9DodccQAXumBNoOvA_pmfBSa9mBSJlElYBsz4RNq2rM130_assertion evidence source_evidence_literature NP417662.RA9DodccQAXumBNoOvA_pmfBSa9mBSJlElYBsz4RNq2rM130_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.