Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP294791.RAHSGMkmogiv8ybmgF-2LEPSd-U2UGSrP2f-3KngBk3dA130_provenance>. }
Showing items 1 to 9 of
9
with 100 items per page.
- source_evidence_literature type ECO_0000212 NP294791.RAHSGMkmogiv8ybmgF-2LEPSd-U2UGSrP2f-3KngBk3dA130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP294791.RAHSGMkmogiv8ybmgF-2LEPSd-U2UGSrP2f-3KngBk3dA130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP294791.RAHSGMkmogiv8ybmgF-2LEPSd-U2UGSrP2f-3KngBk3dA130_provenance.
- NP294791.RAHSGMkmogiv8ybmgF-2LEPSd-U2UGSrP2f-3KngBk3dA130_assertion description "[Familial form of hirschsprung disease: nucleotide sequence studies reveal point mutations in the RET proto-oncogene in two of six families but not in other candidate genes.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP294791.RAHSGMkmogiv8ybmgF-2LEPSd-U2UGSrP2f-3KngBk3dA130_provenance.
- NP294791.RAHSGMkmogiv8ybmgF-2LEPSd-U2UGSrP2f-3KngBk3dA130_assertion evidence source_evidence_literature NP294791.RAHSGMkmogiv8ybmgF-2LEPSd-U2UGSrP2f-3KngBk3dA130_provenance.
- NP294791.RAHSGMkmogiv8ybmgF-2LEPSd-U2UGSrP2f-3KngBk3dA130_assertion SIO_000772 10982477 NP294791.RAHSGMkmogiv8ybmgF-2LEPSd-U2UGSrP2f-3KngBk3dA130_provenance.
- NP294791.RAHSGMkmogiv8ybmgF-2LEPSd-U2UGSrP2f-3KngBk3dA130_assertion wasDerivedFrom befree-2016 NP294791.RAHSGMkmogiv8ybmgF-2LEPSd-U2UGSrP2f-3KngBk3dA130_provenance.
- NP294791.RAHSGMkmogiv8ybmgF-2LEPSd-U2UGSrP2f-3KngBk3dA130_assertion wasGeneratedBy ECO_0000203 NP294791.RAHSGMkmogiv8ybmgF-2LEPSd-U2UGSrP2f-3KngBk3dA130_provenance.
- befree-2016 importedOn "2016-02-19" NP294791.RAHSGMkmogiv8ybmgF-2LEPSd-U2UGSrP2f-3KngBk3dA130_provenance.