Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP213650.RApz-Q5Ns17N1_mh2iiGHQIfllWaSnrDlChaaPD9O9oU8130_provenance>. }
Showing items 1 to 9 of
9
with 100 items per page.
- source_evidence_literature type ECO_0000212 NP213650.RApz-Q5Ns17N1_mh2iiGHQIfllWaSnrDlChaaPD9O9oU8130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP213650.RApz-Q5Ns17N1_mh2iiGHQIfllWaSnrDlChaaPD9O9oU8130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP213650.RApz-Q5Ns17N1_mh2iiGHQIfllWaSnrDlChaaPD9O9oU8130_provenance.
- NP213650.RApz-Q5Ns17N1_mh2iiGHQIfllWaSnrDlChaaPD9O9oU8130_assertion description "[Distinct RB1 gene mutations with low penetrance in hereditary retinoblastoma.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP213650.RApz-Q5Ns17N1_mh2iiGHQIfllWaSnrDlChaaPD9O9oU8130_provenance.
- NP213650.RApz-Q5Ns17N1_mh2iiGHQIfllWaSnrDlChaaPD9O9oU8130_assertion evidence source_evidence_literature NP213650.RApz-Q5Ns17N1_mh2iiGHQIfllWaSnrDlChaaPD9O9oU8130_provenance.
- NP213650.RApz-Q5Ns17N1_mh2iiGHQIfllWaSnrDlChaaPD9O9oU8130_assertion SIO_000772 7927327 NP213650.RApz-Q5Ns17N1_mh2iiGHQIfllWaSnrDlChaaPD9O9oU8130_provenance.
- NP213650.RApz-Q5Ns17N1_mh2iiGHQIfllWaSnrDlChaaPD9O9oU8130_assertion wasDerivedFrom befree-20140225 NP213650.RApz-Q5Ns17N1_mh2iiGHQIfllWaSnrDlChaaPD9O9oU8130_provenance.
- NP213650.RApz-Q5Ns17N1_mh2iiGHQIfllWaSnrDlChaaPD9O9oU8130_assertion wasGeneratedBy ECO_0000203 NP213650.RApz-Q5Ns17N1_mh2iiGHQIfllWaSnrDlChaaPD9O9oU8130_provenance.
- befree-20140225 importedOn "2014-02-25" NP213650.RApz-Q5Ns17N1_mh2iiGHQIfllWaSnrDlChaaPD9O9oU8130_provenance.