Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP1393789.RAkpJgS3P7cRBLeugER53tPRXRUfgIgvTYC7qAhWfc1DE130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP1393789.RAkpJgS3P7cRBLeugER53tPRXRUfgIgvTYC7qAhWfc1DE130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP1393789.RAkpJgS3P7cRBLeugER53tPRXRUfgIgvTYC7qAhWfc1DE130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP1393789.RAkpJgS3P7cRBLeugER53tPRXRUfgIgvTYC7qAhWfc1DE130_provenance.
- 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.
- befree-2016 importedOn "2016-02-19" NP1393789.RAkpJgS3P7cRBLeugER53tPRXRUfgIgvTYC7qAhWfc1DE130_provenance.