Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP249923.RASXiStY0e7pDk1d0gdpZHe0H56HPkqS7pCnH7fRN-Qtg130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP249923.RASXiStY0e7pDk1d0gdpZHe0H56HPkqS7pCnH7fRN-Qtg130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP249923.RASXiStY0e7pDk1d0gdpZHe0H56HPkqS7pCnH7fRN-Qtg130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP249923.RASXiStY0e7pDk1d0gdpZHe0H56HPkqS7pCnH7fRN-Qtg130_provenance.
- NP249923.RASXiStY0e7pDk1d0gdpZHe0H56HPkqS7pCnH7fRN-Qtg130_assertion description "[Seven novel mutations in the adenosine deaminase (ADA) gene in patients with severe and delayed onset combined immunodeficiency: G74C, V129M, G140E, R149W, Q199P, 462delG, and E337del. Mutations in brief no. 142. Online.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP249923.RASXiStY0e7pDk1d0gdpZHe0H56HPkqS7pCnH7fRN-Qtg130_provenance.
- NP249923.RASXiStY0e7pDk1d0gdpZHe0H56HPkqS7pCnH7fRN-Qtg130_assertion evidence source_evidence_literature NP249923.RASXiStY0e7pDk1d0gdpZHe0H56HPkqS7pCnH7fRN-Qtg130_provenance.
- NP249923.RASXiStY0e7pDk1d0gdpZHe0H56HPkqS7pCnH7fRN-Qtg130_assertion SIO_000772 10200056 NP249923.RASXiStY0e7pDk1d0gdpZHe0H56HPkqS7pCnH7fRN-Qtg130_provenance.
- NP249923.RASXiStY0e7pDk1d0gdpZHe0H56HPkqS7pCnH7fRN-Qtg130_assertion wasDerivedFrom befree-2016 NP249923.RASXiStY0e7pDk1d0gdpZHe0H56HPkqS7pCnH7fRN-Qtg130_provenance.
- NP249923.RASXiStY0e7pDk1d0gdpZHe0H56HPkqS7pCnH7fRN-Qtg130_assertion wasGeneratedBy ECO_0000203 NP249923.RASXiStY0e7pDk1d0gdpZHe0H56HPkqS7pCnH7fRN-Qtg130_provenance.
- befree-2016 importedOn "2016-02-19" NP249923.RASXiStY0e7pDk1d0gdpZHe0H56HPkqS7pCnH7fRN-Qtg130_provenance.