Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP4678.RAXyafpnjlmFUohgV0PSapdlb2CXc7aUs9-2N_1Pe4q5s130_assertion> ?p ?o ?g. }
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- NP4678.RAXyafpnjlmFUohgV0PSapdlb2CXc7aUs9-2N_1Pe4q5s130_assertion type Assertion NP4678.RAXyafpnjlmFUohgV0PSapdlb2CXc7aUs9-2N_1Pe4q5s130_head.
- NP4678.RAXyafpnjlmFUohgV0PSapdlb2CXc7aUs9-2N_1Pe4q5s130_assertion wasGeneratedBy ECO_0000218 NP4678.RAXyafpnjlmFUohgV0PSapdlb2CXc7aUs9-2N_1Pe4q5s130_provenance.
- NP4678.RAXyafpnjlmFUohgV0PSapdlb2CXc7aUs9-2N_1Pe4q5s130_assertion wasDerivedFrom uniprot-20150221 NP4678.RAXyafpnjlmFUohgV0PSapdlb2CXc7aUs9-2N_1Pe4q5s130_provenance.
- NP4678.RAXyafpnjlmFUohgV0PSapdlb2CXc7aUs9-2N_1Pe4q5s130_assertion SIO_000772 16385458 NP4678.RAXyafpnjlmFUohgV0PSapdlb2CXc7aUs9-2N_1Pe4q5s130_provenance.
- NP4678.RAXyafpnjlmFUohgV0PSapdlb2CXc7aUs9-2N_1Pe4q5s130_assertion evidence source_evidence_curated NP4678.RAXyafpnjlmFUohgV0PSapdlb2CXc7aUs9-2N_1Pe4q5s130_provenance.
- NP4678.RAXyafpnjlmFUohgV0PSapdlb2CXc7aUs9-2N_1Pe4q5s130_assertion description "[Mutations in a novel isoform of TRIOBP that encodes a filamentous-actin binding protein are responsible for DFNB28 recessive nonsyndromic hearing loss.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP4678.RAXyafpnjlmFUohgV0PSapdlb2CXc7aUs9-2N_1Pe4q5s130_provenance.