Matches in Nanopublications for { <http://rdf.disgenet.org/nanopublications.trig#NP168365.RAMxn6Kh9rFIr789JbHnOHhtpIOlq_coidu6C6ozcNEm0130_assertion> ?p ?o ?g. }
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- NP168365.RAMxn6Kh9rFIr789JbHnOHhtpIOlq_coidu6C6ozcNEm0130_assertion type Assertion NP168365.RAMxn6Kh9rFIr789JbHnOHhtpIOlq_coidu6C6ozcNEm0130_head.
- NP168365.RAMxn6Kh9rFIr789JbHnOHhtpIOlq_coidu6C6ozcNEm0130_assertion description "[Tyrosinase-related oculocutaneous albinism (OCA1), an autosomal recessive inborn error of pigmentation, is caused by the deficiency of tyrosinase.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP168365.RAMxn6Kh9rFIr789JbHnOHhtpIOlq_coidu6C6ozcNEm0130_provenance.
- NP168365.RAMxn6Kh9rFIr789JbHnOHhtpIOlq_coidu6C6ozcNEm0130_assertion evidence source_evidence_literature NP168365.RAMxn6Kh9rFIr789JbHnOHhtpIOlq_coidu6C6ozcNEm0130_provenance.
- NP168365.RAMxn6Kh9rFIr789JbHnOHhtpIOlq_coidu6C6ozcNEm0130_assertion SIO_000772 9560949 NP168365.RAMxn6Kh9rFIr789JbHnOHhtpIOlq_coidu6C6ozcNEm0130_provenance.
- NP168365.RAMxn6Kh9rFIr789JbHnOHhtpIOlq_coidu6C6ozcNEm0130_assertion wasDerivedFrom befree-20140225 NP168365.RAMxn6Kh9rFIr789JbHnOHhtpIOlq_coidu6C6ozcNEm0130_provenance.
- NP168365.RAMxn6Kh9rFIr789JbHnOHhtpIOlq_coidu6C6ozcNEm0130_assertion wasGeneratedBy ECO_0000203 NP168365.RAMxn6Kh9rFIr789JbHnOHhtpIOlq_coidu6C6ozcNEm0130_provenance.