Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP886025.RAb9kMN8QlAcz4Qrtr3Wzkgbp1n2zCPcmwZOQnkCDaaRA130_assertion> ?p ?o ?g. }
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- NP886025.RAb9kMN8QlAcz4Qrtr3Wzkgbp1n2zCPcmwZOQnkCDaaRA130_assertion type Assertion NP886025.RAb9kMN8QlAcz4Qrtr3Wzkgbp1n2zCPcmwZOQnkCDaaRA130_head.
- NP886025.RAb9kMN8QlAcz4Qrtr3Wzkgbp1n2zCPcmwZOQnkCDaaRA130_assertion description "[Although mutations in MYH14 have been shown to cause nonsyndromic autosomal dominant hearing loss (DFNA4), the peripheral neuropathy, myopathy, and hoarseness have not been associated with MYH14.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP886025.RAb9kMN8QlAcz4Qrtr3Wzkgbp1n2zCPcmwZOQnkCDaaRA130_provenance.
- NP886025.RAb9kMN8QlAcz4Qrtr3Wzkgbp1n2zCPcmwZOQnkCDaaRA130_assertion evidence source_evidence_literature NP886025.RAb9kMN8QlAcz4Qrtr3Wzkgbp1n2zCPcmwZOQnkCDaaRA130_provenance.
- NP886025.RAb9kMN8QlAcz4Qrtr3Wzkgbp1n2zCPcmwZOQnkCDaaRA130_assertion SIO_000772 21480433 NP886025.RAb9kMN8QlAcz4Qrtr3Wzkgbp1n2zCPcmwZOQnkCDaaRA130_provenance.
- NP886025.RAb9kMN8QlAcz4Qrtr3Wzkgbp1n2zCPcmwZOQnkCDaaRA130_assertion wasDerivedFrom befree-2016 NP886025.RAb9kMN8QlAcz4Qrtr3Wzkgbp1n2zCPcmwZOQnkCDaaRA130_provenance.
- NP886025.RAb9kMN8QlAcz4Qrtr3Wzkgbp1n2zCPcmwZOQnkCDaaRA130_assertion wasGeneratedBy ECO_0000203 NP886025.RAb9kMN8QlAcz4Qrtr3Wzkgbp1n2zCPcmwZOQnkCDaaRA130_provenance.