Matches in Nanopublications for { <http://rdf.disgenet.org/nanopublications.trig#NP3961.RAdR1CQhLmC_DxpK4a-fdj7L9_VUwIjxPsnijyNyKqPpg130_assertion> ?p ?o ?g. }
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- NP3961.RAdR1CQhLmC_DxpK4a-fdj7L9_VUwIjxPsnijyNyKqPpg130_assertion type Assertion NP3961.RAdR1CQhLmC_DxpK4a-fdj7L9_VUwIjxPsnijyNyKqPpg130_head.
- NP3961.RAdR1CQhLmC_DxpK4a-fdj7L9_VUwIjxPsnijyNyKqPpg130_assertion wasGeneratedBy ECO_0000218 NP3961.RAdR1CQhLmC_DxpK4a-fdj7L9_VUwIjxPsnijyNyKqPpg130_provenance.
- NP3961.RAdR1CQhLmC_DxpK4a-fdj7L9_VUwIjxPsnijyNyKqPpg130_assertion wasDerivedFrom uniprot-20130724 NP3961.RAdR1CQhLmC_DxpK4a-fdj7L9_VUwIjxPsnijyNyKqPpg130_provenance.
- NP3961.RAdR1CQhLmC_DxpK4a-fdj7L9_VUwIjxPsnijyNyKqPpg130_assertion SIO_000772 11406611 NP3961.RAdR1CQhLmC_DxpK4a-fdj7L9_VUwIjxPsnijyNyKqPpg130_provenance.
- NP3961.RAdR1CQhLmC_DxpK4a-fdj7L9_VUwIjxPsnijyNyKqPpg130_assertion evidence source_evidence_curated NP3961.RAdR1CQhLmC_DxpK4a-fdj7L9_VUwIjxPsnijyNyKqPpg130_provenance.
- NP3961.RAdR1CQhLmC_DxpK4a-fdj7L9_VUwIjxPsnijyNyKqPpg130_assertion description "[These data provide evidence that human MCC deficiency is caused by mutations in either the MCCA or MCCB gene.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP3961.RAdR1CQhLmC_DxpK4a-fdj7L9_VUwIjxPsnijyNyKqPpg130_provenance.