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- NP988735.RAxBiSOOMWMgPGvrE7hmUVWO34RV3i9AA51ufrm_HaD5Q130_assertion type Assertion NP988735.RAxBiSOOMWMgPGvrE7hmUVWO34RV3i9AA51ufrm_HaD5Q130_head.
- NP988735.RAxBiSOOMWMgPGvrE7hmUVWO34RV3i9AA51ufrm_HaD5Q130_assertion wasGeneratedBy ECO_0000203 NP988735.RAxBiSOOMWMgPGvrE7hmUVWO34RV3i9AA51ufrm_HaD5Q130_provenance.
- NP988735.RAxBiSOOMWMgPGvrE7hmUVWO34RV3i9AA51ufrm_HaD5Q130_assertion wasDerivedFrom befree-20150227 NP988735.RAxBiSOOMWMgPGvrE7hmUVWO34RV3i9AA51ufrm_HaD5Q130_provenance.
- NP988735.RAxBiSOOMWMgPGvrE7hmUVWO34RV3i9AA51ufrm_HaD5Q130_assertion SIO_000772 19027966 NP988735.RAxBiSOOMWMgPGvrE7hmUVWO34RV3i9AA51ufrm_HaD5Q130_provenance.
- NP988735.RAxBiSOOMWMgPGvrE7hmUVWO34RV3i9AA51ufrm_HaD5Q130_assertion evidence source_evidence_literature NP988735.RAxBiSOOMWMgPGvrE7hmUVWO34RV3i9AA51ufrm_HaD5Q130_provenance.
- NP988735.RAxBiSOOMWMgPGvrE7hmUVWO34RV3i9AA51ufrm_HaD5Q130_assertion description "[Splice variant IVS2-2A>G in the SLC26A5 (Prestin) gene in five Estonian families with hearing loss.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP988735.RAxBiSOOMWMgPGvrE7hmUVWO34RV3i9AA51ufrm_HaD5Q130_provenance.