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- source_evidence_literature type ECO_0000212 NP260827.RA3ViGO6e5m4haerECo7WcXV0V-w3Zx1gUYw3kyp351o8130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP260827.RA3ViGO6e5m4haerECo7WcXV0V-w3Zx1gUYw3kyp351o8130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP260827.RA3ViGO6e5m4haerECo7WcXV0V-w3Zx1gUYw3kyp351o8130_provenance.
- NP260827.RA3ViGO6e5m4haerECo7WcXV0V-w3Zx1gUYw3kyp351o8130_assertion description "[Systematic screening using the SSCP technique followed by sequencing of bands with abnormal mobility derived from the AGXT exons of 15 unrelated Italian patients with primary hyperoxaluria type 1 (PH1) allowed us to characterize both the mutant alleles in each individual.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP260827.RA3ViGO6e5m4haerECo7WcXV0V-w3Zx1gUYw3kyp351o8130_provenance.
- NP260827.RA3ViGO6e5m4haerECo7WcXV0V-w3Zx1gUYw3kyp351o8130_assertion evidence source_evidence_literature NP260827.RA3ViGO6e5m4haerECo7WcXV0V-w3Zx1gUYw3kyp351o8130_provenance.
- NP260827.RA3ViGO6e5m4haerECo7WcXV0V-w3Zx1gUYw3kyp351o8130_assertion SIO_000772 10453743 NP260827.RA3ViGO6e5m4haerECo7WcXV0V-w3Zx1gUYw3kyp351o8130_provenance.
- NP260827.RA3ViGO6e5m4haerECo7WcXV0V-w3Zx1gUYw3kyp351o8130_assertion wasDerivedFrom befree-2016 NP260827.RA3ViGO6e5m4haerECo7WcXV0V-w3Zx1gUYw3kyp351o8130_provenance.
- NP260827.RA3ViGO6e5m4haerECo7WcXV0V-w3Zx1gUYw3kyp351o8130_assertion wasGeneratedBy ECO_0000203 NP260827.RA3ViGO6e5m4haerECo7WcXV0V-w3Zx1gUYw3kyp351o8130_provenance.
- befree-2016 importedOn "2016-02-19" NP260827.RA3ViGO6e5m4haerECo7WcXV0V-w3Zx1gUYw3kyp351o8130_provenance.