Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP364925.RAKFOg8MlrkNNdaLNmiHPwVGuhCQibLR-Pef_EsqBMw9M130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP364925.RAKFOg8MlrkNNdaLNmiHPwVGuhCQibLR-Pef_EsqBMw9M130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP364925.RAKFOg8MlrkNNdaLNmiHPwVGuhCQibLR-Pef_EsqBMw9M130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP364925.RAKFOg8MlrkNNdaLNmiHPwVGuhCQibLR-Pef_EsqBMw9M130_provenance.
- NP364925.RAKFOg8MlrkNNdaLNmiHPwVGuhCQibLR-Pef_EsqBMw9M130_assertion description "[Fabry's disease is an X linked inborn error of metabolism due to deficient activity of the lysosomal enzyme alpha galactosidase A.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP364925.RAKFOg8MlrkNNdaLNmiHPwVGuhCQibLR-Pef_EsqBMw9M130_provenance.
- NP364925.RAKFOg8MlrkNNdaLNmiHPwVGuhCQibLR-Pef_EsqBMw9M130_assertion evidence source_evidence_literature NP364925.RAKFOg8MlrkNNdaLNmiHPwVGuhCQibLR-Pef_EsqBMw9M130_provenance.
- NP364925.RAKFOg8MlrkNNdaLNmiHPwVGuhCQibLR-Pef_EsqBMw9M130_assertion SIO_000772 12185177 NP364925.RAKFOg8MlrkNNdaLNmiHPwVGuhCQibLR-Pef_EsqBMw9M130_provenance.
- NP364925.RAKFOg8MlrkNNdaLNmiHPwVGuhCQibLR-Pef_EsqBMw9M130_assertion wasDerivedFrom befree-2016 NP364925.RAKFOg8MlrkNNdaLNmiHPwVGuhCQibLR-Pef_EsqBMw9M130_provenance.
- NP364925.RAKFOg8MlrkNNdaLNmiHPwVGuhCQibLR-Pef_EsqBMw9M130_assertion wasGeneratedBy ECO_0000203 NP364925.RAKFOg8MlrkNNdaLNmiHPwVGuhCQibLR-Pef_EsqBMw9M130_provenance.
- befree-2016 importedOn "2016-02-19" NP364925.RAKFOg8MlrkNNdaLNmiHPwVGuhCQibLR-Pef_EsqBMw9M130_provenance.