Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP1246738.RArV4XMmtJX1M_CjDM-IC7dOu-UZb1_WbS0yII7K8KHck130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP1246738.RArV4XMmtJX1M_CjDM-IC7dOu-UZb1_WbS0yII7K8KHck130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP1246738.RArV4XMmtJX1M_CjDM-IC7dOu-UZb1_WbS0yII7K8KHck130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP1246738.RArV4XMmtJX1M_CjDM-IC7dOu-UZb1_WbS0yII7K8KHck130_provenance.
- NP1246738.RArV4XMmtJX1M_CjDM-IC7dOu-UZb1_WbS0yII7K8KHck130_assertion description "[In total, 20 of the 50 (40%) T-ALL patients revealed heterozygous mutations in the NOTCH1 domains, and a predominance of missense mutations in HD-N (70%) and PEST (15%) domains.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1246738.RArV4XMmtJX1M_CjDM-IC7dOu-UZb1_WbS0yII7K8KHck130_provenance.
- NP1246738.RArV4XMmtJX1M_CjDM-IC7dOu-UZb1_WbS0yII7K8KHck130_assertion evidence source_evidence_literature NP1246738.RArV4XMmtJX1M_CjDM-IC7dOu-UZb1_WbS0yII7K8KHck130_provenance.
- NP1246738.RArV4XMmtJX1M_CjDM-IC7dOu-UZb1_WbS0yII7K8KHck130_assertion SIO_000772 25493453 NP1246738.RArV4XMmtJX1M_CjDM-IC7dOu-UZb1_WbS0yII7K8KHck130_provenance.
- NP1246738.RArV4XMmtJX1M_CjDM-IC7dOu-UZb1_WbS0yII7K8KHck130_assertion wasDerivedFrom befree-2016 NP1246738.RArV4XMmtJX1M_CjDM-IC7dOu-UZb1_WbS0yII7K8KHck130_provenance.
- NP1246738.RArV4XMmtJX1M_CjDM-IC7dOu-UZb1_WbS0yII7K8KHck130_assertion wasGeneratedBy ECO_0000203 NP1246738.RArV4XMmtJX1M_CjDM-IC7dOu-UZb1_WbS0yII7K8KHck130_provenance.
- befree-2016 importedOn "2016-02-19" NP1246738.RArV4XMmtJX1M_CjDM-IC7dOu-UZb1_WbS0yII7K8KHck130_provenance.