Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP317152.RA4wYhXNhfspQ9dyhGKPvBN_lM71MZWAepREyb8KvesVE130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP317152.RA4wYhXNhfspQ9dyhGKPvBN_lM71MZWAepREyb8KvesVE130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP317152.RA4wYhXNhfspQ9dyhGKPvBN_lM71MZWAepREyb8KvesVE130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP317152.RA4wYhXNhfspQ9dyhGKPvBN_lM71MZWAepREyb8KvesVE130_provenance.
- befree-2016 importedOn "2016-02-19" NP317152.RA4wYhXNhfspQ9dyhGKPvBN_lM71MZWAepREyb8KvesVE130_provenance.
- NP317152.RA4wYhXNhfspQ9dyhGKPvBN_lM71MZWAepREyb8KvesVE130_assertion wasGeneratedBy ECO_0000203 NP317152.RA4wYhXNhfspQ9dyhGKPvBN_lM71MZWAepREyb8KvesVE130_provenance.
- NP317152.RA4wYhXNhfspQ9dyhGKPvBN_lM71MZWAepREyb8KvesVE130_assertion wasDerivedFrom befree-2016 NP317152.RA4wYhXNhfspQ9dyhGKPvBN_lM71MZWAepREyb8KvesVE130_provenance.
- NP317152.RA4wYhXNhfspQ9dyhGKPvBN_lM71MZWAepREyb8KvesVE130_assertion SIO_000772 11342419 NP317152.RA4wYhXNhfspQ9dyhGKPvBN_lM71MZWAepREyb8KvesVE130_provenance.
- NP317152.RA4wYhXNhfspQ9dyhGKPvBN_lM71MZWAepREyb8KvesVE130_assertion evidence source_evidence_literature NP317152.RA4wYhXNhfspQ9dyhGKPvBN_lM71MZWAepREyb8KvesVE130_provenance.
- NP317152.RA4wYhXNhfspQ9dyhGKPvBN_lM71MZWAepREyb8KvesVE130_assertion description "[These variations generally reflect the phenotype of ALAD in vivo in patients with ADP and indicate that GST-ALAD fusion protein is indeed useful for predicting of the phenotype of ALAD mutants.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP317152.RA4wYhXNhfspQ9dyhGKPvBN_lM71MZWAepREyb8KvesVE130_provenance.