Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP1293732.RAizCtthF2O2avuNkmyRF2p2MAh-1IKTay2Guo2MfpjCo130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP1293732.RAizCtthF2O2avuNkmyRF2p2MAh-1IKTay2Guo2MfpjCo130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP1293732.RAizCtthF2O2avuNkmyRF2p2MAh-1IKTay2Guo2MfpjCo130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP1293732.RAizCtthF2O2avuNkmyRF2p2MAh-1IKTay2Guo2MfpjCo130_provenance.
- NP1293732.RAizCtthF2O2avuNkmyRF2p2MAh-1IKTay2Guo2MfpjCo130_assertion description "[PTEN and NOTCH1 mutations were almost mutually exclusive, while IL7R and WT1 mutations were rare in pediatric T-ALL and PTPN11 and AKT1 mutations were infrequent in adult T-ALL.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1293732.RAizCtthF2O2avuNkmyRF2p2MAh-1IKTay2Guo2MfpjCo130_provenance.
- NP1293732.RAizCtthF2O2avuNkmyRF2p2MAh-1IKTay2Guo2MfpjCo130_assertion evidence source_evidence_literature NP1293732.RAizCtthF2O2avuNkmyRF2p2MAh-1IKTay2Guo2MfpjCo130_provenance.
- NP1293732.RAizCtthF2O2avuNkmyRF2p2MAh-1IKTay2Guo2MfpjCo130_assertion SIO_000772 26341754 NP1293732.RAizCtthF2O2avuNkmyRF2p2MAh-1IKTay2Guo2MfpjCo130_provenance.
- NP1293732.RAizCtthF2O2avuNkmyRF2p2MAh-1IKTay2Guo2MfpjCo130_assertion wasDerivedFrom befree-2016 NP1293732.RAizCtthF2O2avuNkmyRF2p2MAh-1IKTay2Guo2MfpjCo130_provenance.
- NP1293732.RAizCtthF2O2avuNkmyRF2p2MAh-1IKTay2Guo2MfpjCo130_assertion wasGeneratedBy ECO_0000203 NP1293732.RAizCtthF2O2avuNkmyRF2p2MAh-1IKTay2Guo2MfpjCo130_provenance.
- befree-2016 importedOn "2016-02-19" NP1293732.RAizCtthF2O2avuNkmyRF2p2MAh-1IKTay2Guo2MfpjCo130_provenance.