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- source_evidence_literature type ECO_0000212 NP853467.RA-cgaVBNWpDlqE8SCkGwdk91KPSK1B9NXYP7-0OxXDkI130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP853467.RA-cgaVBNWpDlqE8SCkGwdk91KPSK1B9NXYP7-0OxXDkI130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP853467.RA-cgaVBNWpDlqE8SCkGwdk91KPSK1B9NXYP7-0OxXDkI130_provenance.
- NP853467.RA-cgaVBNWpDlqE8SCkGwdk91KPSK1B9NXYP7-0OxXDkI130_assertion description "[The absence of the phenotype of hereditary stomatocytosis implies that protein 7.2b deficiency plays no direct role in the etiology of this disorder and casts doubt on the previously proposed role of this protein as a mediator of cation transport in RBC.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP853467.RA-cgaVBNWpDlqE8SCkGwdk91KPSK1B9NXYP7-0OxXDkI130_provenance.
- NP853467.RA-cgaVBNWpDlqE8SCkGwdk91KPSK1B9NXYP7-0OxXDkI130_assertion evidence source_evidence_literature NP853467.RA-cgaVBNWpDlqE8SCkGwdk91KPSK1B9NXYP7-0OxXDkI130_provenance.
- NP853467.RA-cgaVBNWpDlqE8SCkGwdk91KPSK1B9NXYP7-0OxXDkI130_assertion SIO_000772 10090952 NP853467.RA-cgaVBNWpDlqE8SCkGwdk91KPSK1B9NXYP7-0OxXDkI130_provenance.
- NP853467.RA-cgaVBNWpDlqE8SCkGwdk91KPSK1B9NXYP7-0OxXDkI130_assertion wasDerivedFrom befree-20140225 NP853467.RA-cgaVBNWpDlqE8SCkGwdk91KPSK1B9NXYP7-0OxXDkI130_provenance.
- NP853467.RA-cgaVBNWpDlqE8SCkGwdk91KPSK1B9NXYP7-0OxXDkI130_assertion wasGeneratedBy ECO_0000203 NP853467.RA-cgaVBNWpDlqE8SCkGwdk91KPSK1B9NXYP7-0OxXDkI130_provenance.
- befree-20140225 importedOn "2014-02-25" NP853467.RA-cgaVBNWpDlqE8SCkGwdk91KPSK1B9NXYP7-0OxXDkI130_provenance.