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- NP537620.RA_cbUYeOY5bHswWlX0DIwNgVi443zRyNk6oEJ3eswNAU130_assertion type Assertion NP537620.RA_cbUYeOY5bHswWlX0DIwNgVi443zRyNk6oEJ3eswNAU130_head.
- NP537620.RA_cbUYeOY5bHswWlX0DIwNgVi443zRyNk6oEJ3eswNAU130_assertion description "[Mutations in genes encoding myosin VIIa, harmonin, cadherin 23, protocadherin 15 or sans cause Usher syndrome type I (USH1, characterized by congenital deafness, vestibular dysfunction and retinitis pigmentosa leading to blindness) in humans and hair bundle disorganization in mice.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP537620.RA_cbUYeOY5bHswWlX0DIwNgVi443zRyNk6oEJ3eswNAU130_provenance.
- NP537620.RA_cbUYeOY5bHswWlX0DIwNgVi443zRyNk6oEJ3eswNAU130_assertion evidence source_evidence_literature NP537620.RA_cbUYeOY5bHswWlX0DIwNgVi443zRyNk6oEJ3eswNAU130_provenance.
- NP537620.RA_cbUYeOY5bHswWlX0DIwNgVi443zRyNk6oEJ3eswNAU130_assertion SIO_000772 18339676 NP537620.RA_cbUYeOY5bHswWlX0DIwNgVi443zRyNk6oEJ3eswNAU130_provenance.
- NP537620.RA_cbUYeOY5bHswWlX0DIwNgVi443zRyNk6oEJ3eswNAU130_assertion wasDerivedFrom befree-20140225 NP537620.RA_cbUYeOY5bHswWlX0DIwNgVi443zRyNk6oEJ3eswNAU130_provenance.
- NP537620.RA_cbUYeOY5bHswWlX0DIwNgVi443zRyNk6oEJ3eswNAU130_assertion wasGeneratedBy ECO_0000203 NP537620.RA_cbUYeOY5bHswWlX0DIwNgVi443zRyNk6oEJ3eswNAU130_provenance.