Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP978622.RAThIm2XEpQgRD7q5Fss0QvjmtN3nRv60P11XpdBatIp8130_provenance>. }
Showing items 1 to 9 of
9
with 100 items per page.
- source_evidence_literature type ECO_0000212 NP978622.RAThIm2XEpQgRD7q5Fss0QvjmtN3nRv60P11XpdBatIp8130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP978622.RAThIm2XEpQgRD7q5Fss0QvjmtN3nRv60P11XpdBatIp8130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP978622.RAThIm2XEpQgRD7q5Fss0QvjmtN3nRv60P11XpdBatIp8130_provenance.
- NP978622.RAThIm2XEpQgRD7q5Fss0QvjmtN3nRv60P11XpdBatIp8130_assertion description "[Three frameshift mutations of ASXL1 leading to a truncated protein were found in three patients (4%) with late onset JMML displaying also RAS activating mutations.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP978622.RAThIm2XEpQgRD7q5Fss0QvjmtN3nRv60P11XpdBatIp8130_provenance.
- NP978622.RAThIm2XEpQgRD7q5Fss0QvjmtN3nRv60P11XpdBatIp8130_assertion evidence source_evidence_literature NP978622.RAThIm2XEpQgRD7q5Fss0QvjmtN3nRv60P11XpdBatIp8130_provenance.
- NP978622.RAThIm2XEpQgRD7q5Fss0QvjmtN3nRv60P11XpdBatIp8130_assertion SIO_000772 20955399 NP978622.RAThIm2XEpQgRD7q5Fss0QvjmtN3nRv60P11XpdBatIp8130_provenance.
- NP978622.RAThIm2XEpQgRD7q5Fss0QvjmtN3nRv60P11XpdBatIp8130_assertion wasDerivedFrom befree-20150227 NP978622.RAThIm2XEpQgRD7q5Fss0QvjmtN3nRv60P11XpdBatIp8130_provenance.
- NP978622.RAThIm2XEpQgRD7q5Fss0QvjmtN3nRv60P11XpdBatIp8130_assertion wasGeneratedBy ECO_0000203 NP978622.RAThIm2XEpQgRD7q5Fss0QvjmtN3nRv60P11XpdBatIp8130_provenance.
- befree-20150227 importedOn "2015-02-27" NP978622.RAThIm2XEpQgRD7q5Fss0QvjmtN3nRv60P11XpdBatIp8130_provenance.