Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP704777.RAC8_sQ76LnxV-Uu_XlNHRZ1oQtgJ7bxrpIAnxB32WzJY130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP704777.RAC8_sQ76LnxV-Uu_XlNHRZ1oQtgJ7bxrpIAnxB32WzJY130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP704777.RAC8_sQ76LnxV-Uu_XlNHRZ1oQtgJ7bxrpIAnxB32WzJY130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP704777.RAC8_sQ76LnxV-Uu_XlNHRZ1oQtgJ7bxrpIAnxB32WzJY130_provenance.
- NP704777.RAC8_sQ76LnxV-Uu_XlNHRZ1oQtgJ7bxrpIAnxB32WzJY130_assertion description "[After 2006, germline mutations in the KRAS, SOS1, and RAF1 genes were reported to cause Noonan syndrome (NS), in addition to the PTPN11 gene, and now we can find the etiology of disease in approximately 60-70% of NS cases.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP704777.RAC8_sQ76LnxV-Uu_XlNHRZ1oQtgJ7bxrpIAnxB32WzJY130_provenance.
- NP704777.RAC8_sQ76LnxV-Uu_XlNHRZ1oQtgJ7bxrpIAnxB32WzJY130_assertion evidence source_evidence_literature NP704777.RAC8_sQ76LnxV-Uu_XlNHRZ1oQtgJ7bxrpIAnxB32WzJY130_provenance.
- NP704777.RAC8_sQ76LnxV-Uu_XlNHRZ1oQtgJ7bxrpIAnxB32WzJY130_assertion SIO_000772 19020799 NP704777.RAC8_sQ76LnxV-Uu_XlNHRZ1oQtgJ7bxrpIAnxB32WzJY130_provenance.
- NP704777.RAC8_sQ76LnxV-Uu_XlNHRZ1oQtgJ7bxrpIAnxB32WzJY130_assertion wasDerivedFrom befree-2016 NP704777.RAC8_sQ76LnxV-Uu_XlNHRZ1oQtgJ7bxrpIAnxB32WzJY130_provenance.
- NP704777.RAC8_sQ76LnxV-Uu_XlNHRZ1oQtgJ7bxrpIAnxB32WzJY130_assertion wasGeneratedBy ECO_0000203 NP704777.RAC8_sQ76LnxV-Uu_XlNHRZ1oQtgJ7bxrpIAnxB32WzJY130_provenance.
- befree-2016 importedOn "2016-02-19" NP704777.RAC8_sQ76LnxV-Uu_XlNHRZ1oQtgJ7bxrpIAnxB32WzJY130_provenance.