Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP587683.RAyn7EFJkC8vZb7Wzow-JKycVu0R_LFB9ZjR9n3xpAlIM130_assertion> ?p ?o ?g. }
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- NP587683.RAyn7EFJkC8vZb7Wzow-JKycVu0R_LFB9ZjR9n3xpAlIM130_assertion type Assertion NP587683.RAyn7EFJkC8vZb7Wzow-JKycVu0R_LFB9ZjR9n3xpAlIM130_head.
- NP587683.RAyn7EFJkC8vZb7Wzow-JKycVu0R_LFB9ZjR9n3xpAlIM130_assertion description "[Mutations in the connexin 26 (Cx26) or gap junction beta 2 gene are the leading cause of hereditary nonsyndromic sensorineural hearing loss in Caucasians.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP587683.RAyn7EFJkC8vZb7Wzow-JKycVu0R_LFB9ZjR9n3xpAlIM130_provenance.
- NP587683.RAyn7EFJkC8vZb7Wzow-JKycVu0R_LFB9ZjR9n3xpAlIM130_assertion evidence source_evidence_literature NP587683.RAyn7EFJkC8vZb7Wzow-JKycVu0R_LFB9ZjR9n3xpAlIM130_provenance.
- NP587683.RAyn7EFJkC8vZb7Wzow-JKycVu0R_LFB9ZjR9n3xpAlIM130_assertion SIO_000772 15064611 NP587683.RAyn7EFJkC8vZb7Wzow-JKycVu0R_LFB9ZjR9n3xpAlIM130_provenance.
- NP587683.RAyn7EFJkC8vZb7Wzow-JKycVu0R_LFB9ZjR9n3xpAlIM130_assertion wasDerivedFrom befree-20150227 NP587683.RAyn7EFJkC8vZb7Wzow-JKycVu0R_LFB9ZjR9n3xpAlIM130_provenance.
- NP587683.RAyn7EFJkC8vZb7Wzow-JKycVu0R_LFB9ZjR9n3xpAlIM130_assertion wasGeneratedBy ECO_0000203 NP587683.RAyn7EFJkC8vZb7Wzow-JKycVu0R_LFB9ZjR9n3xpAlIM130_provenance.