Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP211850.RA9DPNNiYIpzXBKdstyvz1wCeNzF5z_C0zku4t_6ACQwA130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP211850.RA9DPNNiYIpzXBKdstyvz1wCeNzF5z_C0zku4t_6ACQwA130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP211850.RA9DPNNiYIpzXBKdstyvz1wCeNzF5z_C0zku4t_6ACQwA130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP211850.RA9DPNNiYIpzXBKdstyvz1wCeNzF5z_C0zku4t_6ACQwA130_provenance.
- NP211850.RA9DPNNiYIpzXBKdstyvz1wCeNzF5z_C0zku4t_6ACQwA130_assertion description "[in the investigated Finnish pedigree with hereditary pancreatitis, the PRSS1 mutation R122H is linked with chronic disease; although the SPINK1 mutation (N34S) was also observed in two individuals, it was not linked with the disease]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP211850.RA9DPNNiYIpzXBKdstyvz1wCeNzF5z_C0zku4t_6ACQwA130_provenance.
- NP211850.RA9DPNNiYIpzXBKdstyvz1wCeNzF5z_C0zku4t_6ACQwA130_assertion evidence source_evidence_literature NP211850.RA9DPNNiYIpzXBKdstyvz1wCeNzF5z_C0zku4t_6ACQwA130_provenance.
- NP211850.RA9DPNNiYIpzXBKdstyvz1wCeNzF5z_C0zku4t_6ACQwA130_assertion SIO_000772 17613931 NP211850.RA9DPNNiYIpzXBKdstyvz1wCeNzF5z_C0zku4t_6ACQwA130_provenance.
- NP211850.RA9DPNNiYIpzXBKdstyvz1wCeNzF5z_C0zku4t_6ACQwA130_assertion wasDerivedFrom lhgdn-20090331 NP211850.RA9DPNNiYIpzXBKdstyvz1wCeNzF5z_C0zku4t_6ACQwA130_provenance.
- NP211850.RA9DPNNiYIpzXBKdstyvz1wCeNzF5z_C0zku4t_6ACQwA130_assertion wasGeneratedBy ECO_0000203 NP211850.RA9DPNNiYIpzXBKdstyvz1wCeNzF5z_C0zku4t_6ACQwA130_provenance.
- lhgdn-20090331 importedOn "2009-03-31" NP211850.RA9DPNNiYIpzXBKdstyvz1wCeNzF5z_C0zku4t_6ACQwA130_provenance.