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- NP70096.RAys85RE0sfX-cxmATYcFpIP09DfyO-WFNXJLX17lx9Q0130_assertion type Assertion NP70096.RAys85RE0sfX-cxmATYcFpIP09DfyO-WFNXJLX17lx9Q0130_head.
- NP70096.RAys85RE0sfX-cxmATYcFpIP09DfyO-WFNXJLX17lx9Q0130_assertion description "[Medium-chain acyl-CoA dehydrogenase (MCAD) mutations identified by MS/MS-based prospective screening of newborns differ from those observed in patients with clinical symptoms: identification and characterization of a new, prevalent mutation that results in mild MCAD deficiency.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP70096.RAys85RE0sfX-cxmATYcFpIP09DfyO-WFNXJLX17lx9Q0130_provenance.
- NP70096.RAys85RE0sfX-cxmATYcFpIP09DfyO-WFNXJLX17lx9Q0130_assertion evidence source_evidence_literature NP70096.RAys85RE0sfX-cxmATYcFpIP09DfyO-WFNXJLX17lx9Q0130_provenance.
- NP70096.RAys85RE0sfX-cxmATYcFpIP09DfyO-WFNXJLX17lx9Q0130_assertion SIO_000772 11349232 NP70096.RAys85RE0sfX-cxmATYcFpIP09DfyO-WFNXJLX17lx9Q0130_provenance.
- NP70096.RAys85RE0sfX-cxmATYcFpIP09DfyO-WFNXJLX17lx9Q0130_assertion wasDerivedFrom gad-20150221 NP70096.RAys85RE0sfX-cxmATYcFpIP09DfyO-WFNXJLX17lx9Q0130_provenance.
- NP70096.RAys85RE0sfX-cxmATYcFpIP09DfyO-WFNXJLX17lx9Q0130_assertion wasGeneratedBy ECO_0000203 NP70096.RAys85RE0sfX-cxmATYcFpIP09DfyO-WFNXJLX17lx9Q0130_provenance.