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- NP804979.RA-QoMhb2b9aZcFe7JiXKpMpRqqfTprMA--KfMzyxLtWE130_assertion type Assertion NP804979.RA-QoMhb2b9aZcFe7JiXKpMpRqqfTprMA--KfMzyxLtWE130_head.
- NP804979.RA-QoMhb2b9aZcFe7JiXKpMpRqqfTprMA--KfMzyxLtWE130_assertion description "[Elimination of the native structure and solubility of the hVAPB MSP domain by the Pro56Ser mutation that causes amyotrophic lateral sclerosis.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP804979.RA-QoMhb2b9aZcFe7JiXKpMpRqqfTprMA--KfMzyxLtWE130_provenance.
- NP804979.RA-QoMhb2b9aZcFe7JiXKpMpRqqfTprMA--KfMzyxLtWE130_assertion evidence source_evidence_literature NP804979.RA-QoMhb2b9aZcFe7JiXKpMpRqqfTprMA--KfMzyxLtWE130_provenance.
- NP804979.RA-QoMhb2b9aZcFe7JiXKpMpRqqfTprMA--KfMzyxLtWE130_assertion SIO_000772 20377183 NP804979.RA-QoMhb2b9aZcFe7JiXKpMpRqqfTprMA--KfMzyxLtWE130_provenance.
- NP804979.RA-QoMhb2b9aZcFe7JiXKpMpRqqfTprMA--KfMzyxLtWE130_assertion wasDerivedFrom befree-2016 NP804979.RA-QoMhb2b9aZcFe7JiXKpMpRqqfTprMA--KfMzyxLtWE130_provenance.
- NP804979.RA-QoMhb2b9aZcFe7JiXKpMpRqqfTprMA--KfMzyxLtWE130_assertion wasGeneratedBy ECO_0000203 NP804979.RA-QoMhb2b9aZcFe7JiXKpMpRqqfTprMA--KfMzyxLtWE130_provenance.