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- source_evidence_literature type ECO_0000212 NP395438.RAU0QM93XWlh9j5c5myC5ZG7Uw-THu85MFwrWdCQCgGMk130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP395438.RAU0QM93XWlh9j5c5myC5ZG7Uw-THu85MFwrWdCQCgGMk130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP395438.RAU0QM93XWlh9j5c5myC5ZG7Uw-THu85MFwrWdCQCgGMk130_provenance.
- NP395438.RAU0QM93XWlh9j5c5myC5ZG7Uw-THu85MFwrWdCQCgGMk130_assertion description "[Usher syndrome type II (USH2) is a genetically heterogeneous autosomal recessive disorder with at least three genetic subtypes (USH2A, USH2B, and USH2C) and is classified phenotypically as congenital hearing loss and progressive retinitis pigmentosa.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP395438.RAU0QM93XWlh9j5c5myC5ZG7Uw-THu85MFwrWdCQCgGMk130_provenance.
- NP395438.RAU0QM93XWlh9j5c5myC5ZG7Uw-THu85MFwrWdCQCgGMk130_assertion evidence source_evidence_literature NP395438.RAU0QM93XWlh9j5c5myC5ZG7Uw-THu85MFwrWdCQCgGMk130_provenance.
- NP395438.RAU0QM93XWlh9j5c5myC5ZG7Uw-THu85MFwrWdCQCgGMk130_assertion SIO_000772 14740321 NP395438.RAU0QM93XWlh9j5c5myC5ZG7Uw-THu85MFwrWdCQCgGMk130_provenance.
- NP395438.RAU0QM93XWlh9j5c5myC5ZG7Uw-THu85MFwrWdCQCgGMk130_assertion wasDerivedFrom befree-20140225 NP395438.RAU0QM93XWlh9j5c5myC5ZG7Uw-THu85MFwrWdCQCgGMk130_provenance.
- NP395438.RAU0QM93XWlh9j5c5myC5ZG7Uw-THu85MFwrWdCQCgGMk130_assertion wasGeneratedBy ECO_0000203 NP395438.RAU0QM93XWlh9j5c5myC5ZG7Uw-THu85MFwrWdCQCgGMk130_provenance.
- befree-20140225 importedOn "2014-02-25" NP395438.RAU0QM93XWlh9j5c5myC5ZG7Uw-THu85MFwrWdCQCgGMk130_provenance.