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- NP707897.RANYnQ0oCqvElBg8CDpcWQSyroXnV8iv61kRamTBP_T2Q130_assertion type Assertion NP707897.RANYnQ0oCqvElBg8CDpcWQSyroXnV8iv61kRamTBP_T2Q130_head.
- NP707897.RANYnQ0oCqvElBg8CDpcWQSyroXnV8iv61kRamTBP_T2Q130_assertion wasGeneratedBy ECO_0000203 NP707897.RANYnQ0oCqvElBg8CDpcWQSyroXnV8iv61kRamTBP_T2Q130_provenance.
- NP707897.RANYnQ0oCqvElBg8CDpcWQSyroXnV8iv61kRamTBP_T2Q130_assertion wasDerivedFrom befree-20150227 NP707897.RANYnQ0oCqvElBg8CDpcWQSyroXnV8iv61kRamTBP_T2Q130_provenance.
- NP707897.RANYnQ0oCqvElBg8CDpcWQSyroXnV8iv61kRamTBP_T2Q130_assertion SIO_000772 16543359 NP707897.RANYnQ0oCqvElBg8CDpcWQSyroXnV8iv61kRamTBP_T2Q130_provenance.
- NP707897.RANYnQ0oCqvElBg8CDpcWQSyroXnV8iv61kRamTBP_T2Q130_assertion evidence source_evidence_literature NP707897.RANYnQ0oCqvElBg8CDpcWQSyroXnV8iv61kRamTBP_T2Q130_provenance.
- NP707897.RANYnQ0oCqvElBg8CDpcWQSyroXnV8iv61kRamTBP_T2Q130_assertion description "[SOX2 mutations are known to cause severe bilateral eye malformations but this is the first report implicating loss of function mutations in this transcription factor in oesophageal malformations.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP707897.RANYnQ0oCqvElBg8CDpcWQSyroXnV8iv61kRamTBP_T2Q130_provenance.