Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP70096.RAys85RE0sfX-cxmATYcFpIP09DfyO-WFNXJLX17lx9Q0130_provenance>. }
Showing items 1 to 9 of
9
with 100 items per page.
- source_evidence_literature type ECO_0000212 NP70096.RAys85RE0sfX-cxmATYcFpIP09DfyO-WFNXJLX17lx9Q0130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP70096.RAys85RE0sfX-cxmATYcFpIP09DfyO-WFNXJLX17lx9Q0130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP70096.RAys85RE0sfX-cxmATYcFpIP09DfyO-WFNXJLX17lx9Q0130_provenance.
- gad-20150221 importedOn "2015-02-21" NP70096.RAys85RE0sfX-cxmATYcFpIP09DfyO-WFNXJLX17lx9Q0130_provenance.
- NP70096.RAys85RE0sfX-cxmATYcFpIP09DfyO-WFNXJLX17lx9Q0130_assertion wasGeneratedBy ECO_0000203 NP70096.RAys85RE0sfX-cxmATYcFpIP09DfyO-WFNXJLX17lx9Q0130_provenance.
- NP70096.RAys85RE0sfX-cxmATYcFpIP09DfyO-WFNXJLX17lx9Q0130_assertion wasDerivedFrom gad-20150221 NP70096.RAys85RE0sfX-cxmATYcFpIP09DfyO-WFNXJLX17lx9Q0130_provenance.
- NP70096.RAys85RE0sfX-cxmATYcFpIP09DfyO-WFNXJLX17lx9Q0130_assertion SIO_000772 11349232 NP70096.RAys85RE0sfX-cxmATYcFpIP09DfyO-WFNXJLX17lx9Q0130_provenance.
- NP70096.RAys85RE0sfX-cxmATYcFpIP09DfyO-WFNXJLX17lx9Q0130_assertion evidence source_evidence_literature NP70096.RAys85RE0sfX-cxmATYcFpIP09DfyO-WFNXJLX17lx9Q0130_provenance.
- 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.