Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP925812.RAfSYOeAu0SFBl3_02Y861pGseEVV_imE80m5hlhCikHg130_assertion> ?p ?o ?g. }
Showing items 1 to 6 of
6
with 100 items per page.
- NP925812.RAfSYOeAu0SFBl3_02Y861pGseEVV_imE80m5hlhCikHg130_assertion type Assertion NP925812.RAfSYOeAu0SFBl3_02Y861pGseEVV_imE80m5hlhCikHg130_head.
- NP925812.RAfSYOeAu0SFBl3_02Y861pGseEVV_imE80m5hlhCikHg130_assertion description "[Recessive mutant alleles of MYO7A, USH1C, CDH23, and PCDH15 cause non-syndromic deafness or type 1 Usher syndrome (USH1) characterised by deafness, vestibular areflexia, and vision loss due to retinitis pigmentosa.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP925812.RAfSYOeAu0SFBl3_02Y861pGseEVV_imE80m5hlhCikHg130_provenance.
- NP925812.RAfSYOeAu0SFBl3_02Y861pGseEVV_imE80m5hlhCikHg130_assertion evidence source_evidence_literature NP925812.RAfSYOeAu0SFBl3_02Y861pGseEVV_imE80m5hlhCikHg130_provenance.
- NP925812.RAfSYOeAu0SFBl3_02Y861pGseEVV_imE80m5hlhCikHg130_assertion SIO_000772 21940737 NP925812.RAfSYOeAu0SFBl3_02Y861pGseEVV_imE80m5hlhCikHg130_provenance.
- NP925812.RAfSYOeAu0SFBl3_02Y861pGseEVV_imE80m5hlhCikHg130_assertion wasDerivedFrom befree-2016 NP925812.RAfSYOeAu0SFBl3_02Y861pGseEVV_imE80m5hlhCikHg130_provenance.
- NP925812.RAfSYOeAu0SFBl3_02Y861pGseEVV_imE80m5hlhCikHg130_assertion wasGeneratedBy ECO_0000203 NP925812.RAfSYOeAu0SFBl3_02Y861pGseEVV_imE80m5hlhCikHg130_provenance.