Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP168365.RAMxn6Kh9rFIr789JbHnOHhtpIOlq_coidu6C6ozcNEm0130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP168365.RAMxn6Kh9rFIr789JbHnOHhtpIOlq_coidu6C6ozcNEm0130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP168365.RAMxn6Kh9rFIr789JbHnOHhtpIOlq_coidu6C6ozcNEm0130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP168365.RAMxn6Kh9rFIr789JbHnOHhtpIOlq_coidu6C6ozcNEm0130_provenance.
- 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.
- befree-20140225 importedOn "2014-02-25" NP168365.RAMxn6Kh9rFIr789JbHnOHhtpIOlq_coidu6C6ozcNEm0130_provenance.