Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP1249025.RAwYxZ6_Yz1pYhdcbKC2xRa77-9fn3SRzLzGHf2hvtaI0130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP1249025.RAwYxZ6_Yz1pYhdcbKC2xRa77-9fn3SRzLzGHf2hvtaI0130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP1249025.RAwYxZ6_Yz1pYhdcbKC2xRa77-9fn3SRzLzGHf2hvtaI0130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP1249025.RAwYxZ6_Yz1pYhdcbKC2xRa77-9fn3SRzLzGHf2hvtaI0130_provenance.
- NP1249025.RAwYxZ6_Yz1pYhdcbKC2xRa77-9fn3SRzLzGHf2hvtaI0130_assertion description "[Although extremely rare, TSC and autosomal dominant polycystic kidney disease (ADPKD) can co-exist in the same patient as a result of concurrent deletion of both polycystic kidney disease (PKD) 1 and TSC2 genes present on the chromosome 16p13.3.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1249025.RAwYxZ6_Yz1pYhdcbKC2xRa77-9fn3SRzLzGHf2hvtaI0130_provenance.
- NP1249025.RAwYxZ6_Yz1pYhdcbKC2xRa77-9fn3SRzLzGHf2hvtaI0130_assertion evidence source_evidence_literature NP1249025.RAwYxZ6_Yz1pYhdcbKC2xRa77-9fn3SRzLzGHf2hvtaI0130_provenance.
- NP1249025.RAwYxZ6_Yz1pYhdcbKC2xRa77-9fn3SRzLzGHf2hvtaI0130_assertion SIO_000772 25519866 NP1249025.RAwYxZ6_Yz1pYhdcbKC2xRa77-9fn3SRzLzGHf2hvtaI0130_provenance.
- NP1249025.RAwYxZ6_Yz1pYhdcbKC2xRa77-9fn3SRzLzGHf2hvtaI0130_assertion wasDerivedFrom befree-2016 NP1249025.RAwYxZ6_Yz1pYhdcbKC2xRa77-9fn3SRzLzGHf2hvtaI0130_provenance.
- NP1249025.RAwYxZ6_Yz1pYhdcbKC2xRa77-9fn3SRzLzGHf2hvtaI0130_assertion wasGeneratedBy ECO_0000203 NP1249025.RAwYxZ6_Yz1pYhdcbKC2xRa77-9fn3SRzLzGHf2hvtaI0130_provenance.
- befree-2016 importedOn "2016-02-19" NP1249025.RAwYxZ6_Yz1pYhdcbKC2xRa77-9fn3SRzLzGHf2hvtaI0130_provenance.