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- source_evidence_literature type ECO_0000212 NP720060.RAbk6fDpEmBdbElSXhTkzhAS5aj4s73njs7kgorODfLQ0130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP720060.RAbk6fDpEmBdbElSXhTkzhAS5aj4s73njs7kgorODfLQ0130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP720060.RAbk6fDpEmBdbElSXhTkzhAS5aj4s73njs7kgorODfLQ0130_provenance.
- NP720060.RAbk6fDpEmBdbElSXhTkzhAS5aj4s73njs7kgorODfLQ0130_assertion description "[Meckel-Gruber syndrome type 3 (MKS3; OMIM 607361) is a severe autosomal recessive disorder characterized by bilateral polycystic kidney disease.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP720060.RAbk6fDpEmBdbElSXhTkzhAS5aj4s73njs7kgorODfLQ0130_provenance.
- NP720060.RAbk6fDpEmBdbElSXhTkzhAS5aj4s73njs7kgorODfLQ0130_assertion evidence source_evidence_literature NP720060.RAbk6fDpEmBdbElSXhTkzhAS5aj4s73njs7kgorODfLQ0130_provenance.
- NP720060.RAbk6fDpEmBdbElSXhTkzhAS5aj4s73njs7kgorODfLQ0130_assertion SIO_000772 19211713 NP720060.RAbk6fDpEmBdbElSXhTkzhAS5aj4s73njs7kgorODfLQ0130_provenance.
- NP720060.RAbk6fDpEmBdbElSXhTkzhAS5aj4s73njs7kgorODfLQ0130_assertion wasDerivedFrom befree-2016 NP720060.RAbk6fDpEmBdbElSXhTkzhAS5aj4s73njs7kgorODfLQ0130_provenance.
- NP720060.RAbk6fDpEmBdbElSXhTkzhAS5aj4s73njs7kgorODfLQ0130_assertion wasGeneratedBy ECO_0000203 NP720060.RAbk6fDpEmBdbElSXhTkzhAS5aj4s73njs7kgorODfLQ0130_provenance.
- befree-2016 importedOn "2016-02-19" NP720060.RAbk6fDpEmBdbElSXhTkzhAS5aj4s73njs7kgorODfLQ0130_provenance.