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- NP682931.RARlC9g8MTfjViWvJLjHGD6aN95lmudjtDrJDjjeQLeSk130_assertion type Assertion NP682931.RARlC9g8MTfjViWvJLjHGD6aN95lmudjtDrJDjjeQLeSk130_head.
- NP682931.RARlC9g8MTfjViWvJLjHGD6aN95lmudjtDrJDjjeQLeSk130_assertion wasGeneratedBy ECO_0000203 NP682931.RARlC9g8MTfjViWvJLjHGD6aN95lmudjtDrJDjjeQLeSk130_provenance.
- NP682931.RARlC9g8MTfjViWvJLjHGD6aN95lmudjtDrJDjjeQLeSk130_assertion wasDerivedFrom befree-20140225 NP682931.RARlC9g8MTfjViWvJLjHGD6aN95lmudjtDrJDjjeQLeSk130_provenance.
- NP682931.RARlC9g8MTfjViWvJLjHGD6aN95lmudjtDrJDjjeQLeSk130_assertion SIO_000772 12107438 NP682931.RARlC9g8MTfjViWvJLjHGD6aN95lmudjtDrJDjjeQLeSk130_provenance.
- NP682931.RARlC9g8MTfjViWvJLjHGD6aN95lmudjtDrJDjjeQLeSk130_assertion evidence source_evidence_literature NP682931.RARlC9g8MTfjViWvJLjHGD6aN95lmudjtDrJDjjeQLeSk130_provenance.
- NP682931.RARlC9g8MTfjViWvJLjHGD6aN95lmudjtDrJDjjeQLeSk130_assertion description "[We found an IVS12+5G-->C mutation in the USHIC gene, which is associated with nonsyndromic recessive deafness ( DFNB18) segregating in the original family, S-11/12.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP682931.RARlC9g8MTfjViWvJLjHGD6aN95lmudjtDrJDjjeQLeSk130_provenance.