Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP434696.RA6KoA0EVr5ay1yTPCqR_lVFdO_JleGB4p-9al8mOboG0130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP434696.RA6KoA0EVr5ay1yTPCqR_lVFdO_JleGB4p-9al8mOboG0130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP434696.RA6KoA0EVr5ay1yTPCqR_lVFdO_JleGB4p-9al8mOboG0130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP434696.RA6KoA0EVr5ay1yTPCqR_lVFdO_JleGB4p-9al8mOboG0130_provenance.
- NP434696.RA6KoA0EVr5ay1yTPCqR_lVFdO_JleGB4p-9al8mOboG0130_assertion description "[A TSC2-PKD1 contiguous gene syndrome caused by chromosomal microdeletions disrupting both the TSC2 and PKD1 genes has been identified in patients with TSC and early-onset severe ADPKD.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP434696.RA6KoA0EVr5ay1yTPCqR_lVFdO_JleGB4p-9al8mOboG0130_provenance.
- NP434696.RA6KoA0EVr5ay1yTPCqR_lVFdO_JleGB4p-9al8mOboG0130_assertion evidence source_evidence_literature NP434696.RA6KoA0EVr5ay1yTPCqR_lVFdO_JleGB4p-9al8mOboG0130_provenance.
- NP434696.RA6KoA0EVr5ay1yTPCqR_lVFdO_JleGB4p-9al8mOboG0130_assertion SIO_000772 15007723 NP434696.RA6KoA0EVr5ay1yTPCqR_lVFdO_JleGB4p-9al8mOboG0130_provenance.
- NP434696.RA6KoA0EVr5ay1yTPCqR_lVFdO_JleGB4p-9al8mOboG0130_assertion wasDerivedFrom befree-2016 NP434696.RA6KoA0EVr5ay1yTPCqR_lVFdO_JleGB4p-9al8mOboG0130_provenance.
- NP434696.RA6KoA0EVr5ay1yTPCqR_lVFdO_JleGB4p-9al8mOboG0130_assertion wasGeneratedBy ECO_0000203 NP434696.RA6KoA0EVr5ay1yTPCqR_lVFdO_JleGB4p-9al8mOboG0130_provenance.
- befree-2016 importedOn "2016-02-19" NP434696.RA6KoA0EVr5ay1yTPCqR_lVFdO_JleGB4p-9al8mOboG0130_provenance.