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- source_evidence_literature type ECO_0000212 NP671477.RAfjb6UeIE9p8fibJQshDSlFTrTE1k_U9224SZ5g2swiE130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP671477.RAfjb6UeIE9p8fibJQshDSlFTrTE1k_U9224SZ5g2swiE130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP671477.RAfjb6UeIE9p8fibJQshDSlFTrTE1k_U9224SZ5g2swiE130_provenance.
- NP671477.RAfjb6UeIE9p8fibJQshDSlFTrTE1k_U9224SZ5g2swiE130_assertion description "[Mutations in the Usher syndrome type I causing genes are also recorded in non-syndromic hearing loss cases and mutations in USH2A in non-syndromic retinitis pigmentosa.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP671477.RAfjb6UeIE9p8fibJQshDSlFTrTE1k_U9224SZ5g2swiE130_provenance.
- NP671477.RAfjb6UeIE9p8fibJQshDSlFTrTE1k_U9224SZ5g2swiE130_assertion evidence source_evidence_literature NP671477.RAfjb6UeIE9p8fibJQshDSlFTrTE1k_U9224SZ5g2swiE130_provenance.
- NP671477.RAfjb6UeIE9p8fibJQshDSlFTrTE1k_U9224SZ5g2swiE130_assertion SIO_000772 18484607 NP671477.RAfjb6UeIE9p8fibJQshDSlFTrTE1k_U9224SZ5g2swiE130_provenance.
- NP671477.RAfjb6UeIE9p8fibJQshDSlFTrTE1k_U9224SZ5g2swiE130_assertion wasDerivedFrom befree-2016 NP671477.RAfjb6UeIE9p8fibJQshDSlFTrTE1k_U9224SZ5g2swiE130_provenance.
- NP671477.RAfjb6UeIE9p8fibJQshDSlFTrTE1k_U9224SZ5g2swiE130_assertion wasGeneratedBy ECO_0000203 NP671477.RAfjb6UeIE9p8fibJQshDSlFTrTE1k_U9224SZ5g2swiE130_provenance.
- befree-2016 importedOn "2016-02-19" NP671477.RAfjb6UeIE9p8fibJQshDSlFTrTE1k_U9224SZ5g2swiE130_provenance.