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- source_evidence_literature type ECO_0000212 NP1066786.RAXqz3eofJV3YVABtgE9xjfc9uX_e7r_6WWa3YI4dAbyk130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP1066786.RAXqz3eofJV3YVABtgE9xjfc9uX_e7r_6WWa3YI4dAbyk130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP1066786.RAXqz3eofJV3YVABtgE9xjfc9uX_e7r_6WWa3YI4dAbyk130_provenance.
- NP1066786.RAXqz3eofJV3YVABtgE9xjfc9uX_e7r_6WWa3YI4dAbyk130_assertion description "[Novel compound heterozygous mutations in MYO7A in a Chinese family with Usher syndrome type 1.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1066786.RAXqz3eofJV3YVABtgE9xjfc9uX_e7r_6WWa3YI4dAbyk130_provenance.
- NP1066786.RAXqz3eofJV3YVABtgE9xjfc9uX_e7r_6WWa3YI4dAbyk130_assertion evidence source_evidence_literature NP1066786.RAXqz3eofJV3YVABtgE9xjfc9uX_e7r_6WWa3YI4dAbyk130_provenance.
- NP1066786.RAXqz3eofJV3YVABtgE9xjfc9uX_e7r_6WWa3YI4dAbyk130_assertion SIO_000772 23559863 NP1066786.RAXqz3eofJV3YVABtgE9xjfc9uX_e7r_6WWa3YI4dAbyk130_provenance.
- NP1066786.RAXqz3eofJV3YVABtgE9xjfc9uX_e7r_6WWa3YI4dAbyk130_assertion wasDerivedFrom befree-2016 NP1066786.RAXqz3eofJV3YVABtgE9xjfc9uX_e7r_6WWa3YI4dAbyk130_provenance.
- NP1066786.RAXqz3eofJV3YVABtgE9xjfc9uX_e7r_6WWa3YI4dAbyk130_assertion wasGeneratedBy ECO_0000203 NP1066786.RAXqz3eofJV3YVABtgE9xjfc9uX_e7r_6WWa3YI4dAbyk130_provenance.
- befree-2016 importedOn "2016-02-19" NP1066786.RAXqz3eofJV3YVABtgE9xjfc9uX_e7r_6WWa3YI4dAbyk130_provenance.