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- source_evidence_literature type ECO_0000212 NP639319.RA5YEazImoHje2kaOdyfB09k955VIKGmgdRGEFZXaK0Uc130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP639319.RA5YEazImoHje2kaOdyfB09k955VIKGmgdRGEFZXaK0Uc130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP639319.RA5YEazImoHje2kaOdyfB09k955VIKGmgdRGEFZXaK0Uc130_provenance.
- NP639319.RA5YEazImoHje2kaOdyfB09k955VIKGmgdRGEFZXaK0Uc130_assertion description "[We have identified 11 different previously unreported mutations in ALOX12B and ALOXE3 in 21 ARCI patients from 19 unrelated families and demonstrated that mutations in the two genes are the second most common cause for ARCI in this cohort of patients.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP639319.RA5YEazImoHje2kaOdyfB09k955VIKGmgdRGEFZXaK0Uc130_provenance.
- NP639319.RA5YEazImoHje2kaOdyfB09k955VIKGmgdRGEFZXaK0Uc130_assertion evidence source_evidence_literature NP639319.RA5YEazImoHje2kaOdyfB09k955VIKGmgdRGEFZXaK0Uc130_provenance.
- NP639319.RA5YEazImoHje2kaOdyfB09k955VIKGmgdRGEFZXaK0Uc130_assertion SIO_000772 19131948 NP639319.RA5YEazImoHje2kaOdyfB09k955VIKGmgdRGEFZXaK0Uc130_provenance.
- NP639319.RA5YEazImoHje2kaOdyfB09k955VIKGmgdRGEFZXaK0Uc130_assertion wasDerivedFrom befree-20140225 NP639319.RA5YEazImoHje2kaOdyfB09k955VIKGmgdRGEFZXaK0Uc130_provenance.
- NP639319.RA5YEazImoHje2kaOdyfB09k955VIKGmgdRGEFZXaK0Uc130_assertion wasGeneratedBy ECO_0000203 NP639319.RA5YEazImoHje2kaOdyfB09k955VIKGmgdRGEFZXaK0Uc130_provenance.
- befree-20140225 importedOn "2014-02-25" NP639319.RA5YEazImoHje2kaOdyfB09k955VIKGmgdRGEFZXaK0Uc130_provenance.