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- source_evidence_literature type ECO_0000212 NP968622.RAQE4FGqW-Pnn2efTTDQ_BdW-aah0DwTPZZuDis1HhksE130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP968622.RAQE4FGqW-Pnn2efTTDQ_BdW-aah0DwTPZZuDis1HhksE130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP968622.RAQE4FGqW-Pnn2efTTDQ_BdW-aah0DwTPZZuDis1HhksE130_provenance.
- NP968622.RAQE4FGqW-Pnn2efTTDQ_BdW-aah0DwTPZZuDis1HhksE130_assertion description "[Some features of GPS[+] overlap with Stargardt disease (STGD1), a recessive macular dystrophy caused by biallelic sequence variants in the ATP-binding cassette transporter 4 (ABCA4) gene.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP968622.RAQE4FGqW-Pnn2efTTDQ_BdW-aah0DwTPZZuDis1HhksE130_provenance.
- NP968622.RAQE4FGqW-Pnn2efTTDQ_BdW-aah0DwTPZZuDis1HhksE130_assertion evidence source_evidence_literature NP968622.RAQE4FGqW-Pnn2efTTDQ_BdW-aah0DwTPZZuDis1HhksE130_provenance.
- NP968622.RAQE4FGqW-Pnn2efTTDQ_BdW-aah0DwTPZZuDis1HhksE130_assertion SIO_000772 22427542 NP968622.RAQE4FGqW-Pnn2efTTDQ_BdW-aah0DwTPZZuDis1HhksE130_provenance.
- NP968622.RAQE4FGqW-Pnn2efTTDQ_BdW-aah0DwTPZZuDis1HhksE130_assertion wasDerivedFrom befree-2016 NP968622.RAQE4FGqW-Pnn2efTTDQ_BdW-aah0DwTPZZuDis1HhksE130_provenance.
- NP968622.RAQE4FGqW-Pnn2efTTDQ_BdW-aah0DwTPZZuDis1HhksE130_assertion wasGeneratedBy ECO_0000203 NP968622.RAQE4FGqW-Pnn2efTTDQ_BdW-aah0DwTPZZuDis1HhksE130_provenance.
- befree-2016 importedOn "2016-02-19" NP968622.RAQE4FGqW-Pnn2efTTDQ_BdW-aah0DwTPZZuDis1HhksE130_provenance.