Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP390845.RAdyWLDJEiYOZax-nZRS2eCXsGX6ceIyIYrJodevUWh98130_assertion> ?p ?o ?g. }
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- NP390845.RAdyWLDJEiYOZax-nZRS2eCXsGX6ceIyIYrJodevUWh98130_assertion type Assertion NP390845.RAdyWLDJEiYOZax-nZRS2eCXsGX6ceIyIYrJodevUWh98130_head.
- NP390845.RAdyWLDJEiYOZax-nZRS2eCXsGX6ceIyIYrJodevUWh98130_assertion wasGeneratedBy ECO_0000203 NP390845.RAdyWLDJEiYOZax-nZRS2eCXsGX6ceIyIYrJodevUWh98130_provenance.
- NP390845.RAdyWLDJEiYOZax-nZRS2eCXsGX6ceIyIYrJodevUWh98130_assertion wasDerivedFrom befree-2016 NP390845.RAdyWLDJEiYOZax-nZRS2eCXsGX6ceIyIYrJodevUWh98130_provenance.
- NP390845.RAdyWLDJEiYOZax-nZRS2eCXsGX6ceIyIYrJodevUWh98130_assertion SIO_000772 12694189 NP390845.RAdyWLDJEiYOZax-nZRS2eCXsGX6ceIyIYrJodevUWh98130_provenance.
- NP390845.RAdyWLDJEiYOZax-nZRS2eCXsGX6ceIyIYrJodevUWh98130_assertion evidence source_evidence_literature NP390845.RAdyWLDJEiYOZax-nZRS2eCXsGX6ceIyIYrJodevUWh98130_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.