Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP657334.RAVDp6OAG5iorhMTupCOZoEMI7VZ0P36-ZRG59Xp7s17M130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP657334.RAVDp6OAG5iorhMTupCOZoEMI7VZ0P36-ZRG59Xp7s17M130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP657334.RAVDp6OAG5iorhMTupCOZoEMI7VZ0P36-ZRG59Xp7s17M130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP657334.RAVDp6OAG5iorhMTupCOZoEMI7VZ0P36-ZRG59Xp7s17M130_provenance.
- NP657334.RAVDp6OAG5iorhMTupCOZoEMI7VZ0P36-ZRG59Xp7s17M130_assertion description "[Nucleotide sequencing of the highly conserved SMPD3 gene in a large panel of human cancers revealed mutations in 5 (5%) of 92 acute myeloid leukemias (AMLs) and 8 (6%) of 131 acute lymphoid leukemias (ALLs), but not in other tumor types.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP657334.RAVDp6OAG5iorhMTupCOZoEMI7VZ0P36-ZRG59Xp7s17M130_provenance.
- NP657334.RAVDp6OAG5iorhMTupCOZoEMI7VZ0P36-ZRG59Xp7s17M130_assertion evidence source_evidence_literature NP657334.RAVDp6OAG5iorhMTupCOZoEMI7VZ0P36-ZRG59Xp7s17M130_provenance.
- NP657334.RAVDp6OAG5iorhMTupCOZoEMI7VZ0P36-ZRG59Xp7s17M130_assertion SIO_000772 18299447 NP657334.RAVDp6OAG5iorhMTupCOZoEMI7VZ0P36-ZRG59Xp7s17M130_provenance.
- NP657334.RAVDp6OAG5iorhMTupCOZoEMI7VZ0P36-ZRG59Xp7s17M130_assertion wasDerivedFrom befree-2016 NP657334.RAVDp6OAG5iorhMTupCOZoEMI7VZ0P36-ZRG59Xp7s17M130_provenance.
- NP657334.RAVDp6OAG5iorhMTupCOZoEMI7VZ0P36-ZRG59Xp7s17M130_assertion wasGeneratedBy ECO_0000203 NP657334.RAVDp6OAG5iorhMTupCOZoEMI7VZ0P36-ZRG59Xp7s17M130_provenance.
- befree-2016 importedOn "2016-02-19" NP657334.RAVDp6OAG5iorhMTupCOZoEMI7VZ0P36-ZRG59Xp7s17M130_provenance.