Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP1393789.RAkpJgS3P7cRBLeugER53tPRXRUfgIgvTYC7qAhWfc1DE130_assertion> ?p ?o ?g. }
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- NP1393789.RAkpJgS3P7cRBLeugER53tPRXRUfgIgvTYC7qAhWfc1DE130_assertion type Assertion NP1393789.RAkpJgS3P7cRBLeugER53tPRXRUfgIgvTYC7qAhWfc1DE130_head.
- NP1393789.RAkpJgS3P7cRBLeugER53tPRXRUfgIgvTYC7qAhWfc1DE130_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." NP1393789.RAkpJgS3P7cRBLeugER53tPRXRUfgIgvTYC7qAhWfc1DE130_provenance.
- NP1393789.RAkpJgS3P7cRBLeugER53tPRXRUfgIgvTYC7qAhWfc1DE130_assertion evidence source_evidence_literature NP1393789.RAkpJgS3P7cRBLeugER53tPRXRUfgIgvTYC7qAhWfc1DE130_provenance.
- NP1393789.RAkpJgS3P7cRBLeugER53tPRXRUfgIgvTYC7qAhWfc1DE130_assertion SIO_000772 9560949 NP1393789.RAkpJgS3P7cRBLeugER53tPRXRUfgIgvTYC7qAhWfc1DE130_provenance.
- NP1393789.RAkpJgS3P7cRBLeugER53tPRXRUfgIgvTYC7qAhWfc1DE130_assertion wasDerivedFrom befree-2016 NP1393789.RAkpJgS3P7cRBLeugER53tPRXRUfgIgvTYC7qAhWfc1DE130_provenance.
- NP1393789.RAkpJgS3P7cRBLeugER53tPRXRUfgIgvTYC7qAhWfc1DE130_assertion wasGeneratedBy ECO_0000203 NP1393789.RAkpJgS3P7cRBLeugER53tPRXRUfgIgvTYC7qAhWfc1DE130_provenance.