Matches in Nanopublications for { <http://rdf.disgenet.org/nanopublications.trig#NP413353.RA1CxGIcUf4zd8VkLr6u6SHQfzv0ubzAs80GvDiLc76FQ130_assertion> ?p ?o ?g. }
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- NP413353.RA1CxGIcUf4zd8VkLr6u6SHQfzv0ubzAs80GvDiLc76FQ130_assertion type Assertion NP413353.RA1CxGIcUf4zd8VkLr6u6SHQfzv0ubzAs80GvDiLc76FQ130_head.
- NP413353.RA1CxGIcUf4zd8VkLr6u6SHQfzv0ubzAs80GvDiLc76FQ130_assertion description "[OCA3 (MIM 203290), a rare form of OCA and also known as `rufous/red albinism,` is associated with mutations in TYRP1 (encoding tyrosinase-related protein 1).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP413353.RA1CxGIcUf4zd8VkLr6u6SHQfzv0ubzAs80GvDiLc76FQ130_provenance.
- NP413353.RA1CxGIcUf4zd8VkLr6u6SHQfzv0ubzAs80GvDiLc76FQ130_assertion evidence source_evidence_literature NP413353.RA1CxGIcUf4zd8VkLr6u6SHQfzv0ubzAs80GvDiLc76FQ130_provenance.
- NP413353.RA1CxGIcUf4zd8VkLr6u6SHQfzv0ubzAs80GvDiLc76FQ130_assertion SIO_000772 11574907 NP413353.RA1CxGIcUf4zd8VkLr6u6SHQfzv0ubzAs80GvDiLc76FQ130_provenance.
- NP413353.RA1CxGIcUf4zd8VkLr6u6SHQfzv0ubzAs80GvDiLc76FQ130_assertion wasDerivedFrom befree-20140225 NP413353.RA1CxGIcUf4zd8VkLr6u6SHQfzv0ubzAs80GvDiLc76FQ130_provenance.
- NP413353.RA1CxGIcUf4zd8VkLr6u6SHQfzv0ubzAs80GvDiLc76FQ130_assertion wasGeneratedBy ECO_0000203 NP413353.RA1CxGIcUf4zd8VkLr6u6SHQfzv0ubzAs80GvDiLc76FQ130_provenance.