Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP339791.RAsV8BXBXDz2-rHkTHw_pRNbhlqPipLALkxbip1A8Ho-s130_provenance>. }
Showing items 1 to 9 of
9
with 100 items per page.
- source_evidence_literature type ECO_0000212 NP339791.RAsV8BXBXDz2-rHkTHw_pRNbhlqPipLALkxbip1A8Ho-s130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP339791.RAsV8BXBXDz2-rHkTHw_pRNbhlqPipLALkxbip1A8Ho-s130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP339791.RAsV8BXBXDz2-rHkTHw_pRNbhlqPipLALkxbip1A8Ho-s130_provenance.
- NP339791.RAsV8BXBXDz2-rHkTHw_pRNbhlqPipLALkxbip1A8Ho-s130_assertion wasGeneratedBy ECO_0000203 NP339791.RAsV8BXBXDz2-rHkTHw_pRNbhlqPipLALkxbip1A8Ho-s130_provenance.
- NP339791.RAsV8BXBXDz2-rHkTHw_pRNbhlqPipLALkxbip1A8Ho-s130_assertion wasDerivedFrom befree-20140225 NP339791.RAsV8BXBXDz2-rHkTHw_pRNbhlqPipLALkxbip1A8Ho-s130_provenance.
- NP339791.RAsV8BXBXDz2-rHkTHw_pRNbhlqPipLALkxbip1A8Ho-s130_assertion SIO_000772 2479409 NP339791.RAsV8BXBXDz2-rHkTHw_pRNbhlqPipLALkxbip1A8Ho-s130_provenance.
- NP339791.RAsV8BXBXDz2-rHkTHw_pRNbhlqPipLALkxbip1A8Ho-s130_assertion evidence source_evidence_literature NP339791.RAsV8BXBXDz2-rHkTHw_pRNbhlqPipLALkxbip1A8Ho-s130_provenance.
- NP339791.RAsV8BXBXDz2-rHkTHw_pRNbhlqPipLALkxbip1A8Ho-s130_assertion description "[Interestingly, the chromosome abnormality of del(1)(p22----pter) near the region of 1p21, where the amylase gene was assigned, was noticed in as many as 76% of KMS-12-PE cells.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP339791.RAsV8BXBXDz2-rHkTHw_pRNbhlqPipLALkxbip1A8Ho-s130_provenance.
- befree-20140225 importedOn "2014-02-25" NP339791.RAsV8BXBXDz2-rHkTHw_pRNbhlqPipLALkxbip1A8Ho-s130_provenance.