Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP274938.RA5IjPVbERfHRJ2Jp5QlXC-o3R7ihtKN3Fo24KnirjYc4130_provenance>. }
Showing items 1 to 9 of
9
with 100 items per page.
- source_evidence_literature type ECO_0000212 NP274938.RA5IjPVbERfHRJ2Jp5QlXC-o3R7ihtKN3Fo24KnirjYc4130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP274938.RA5IjPVbERfHRJ2Jp5QlXC-o3R7ihtKN3Fo24KnirjYc4130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP274938.RA5IjPVbERfHRJ2Jp5QlXC-o3R7ihtKN3Fo24KnirjYc4130_provenance.
- NP274938.RA5IjPVbERfHRJ2Jp5QlXC-o3R7ihtKN3Fo24KnirjYc4130_assertion description "[A PCR technique was used to assay for the null genotype for GSTM1 and GSTT1 in 302 children with ALL, 57 of whom also subsequently developed treatment-related acute myeloid leukemia or myelodysplastic syndrome.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP274938.RA5IjPVbERfHRJ2Jp5QlXC-o3R7ihtKN3Fo24KnirjYc4130_provenance.
- NP274938.RA5IjPVbERfHRJ2Jp5QlXC-o3R7ihtKN3Fo24KnirjYc4130_assertion evidence source_evidence_literature NP274938.RA5IjPVbERfHRJ2Jp5QlXC-o3R7ihtKN3Fo24KnirjYc4130_provenance.
- NP274938.RA5IjPVbERfHRJ2Jp5QlXC-o3R7ihtKN3Fo24KnirjYc4130_assertion SIO_000772 10673738 NP274938.RA5IjPVbERfHRJ2Jp5QlXC-o3R7ihtKN3Fo24KnirjYc4130_provenance.
- NP274938.RA5IjPVbERfHRJ2Jp5QlXC-o3R7ihtKN3Fo24KnirjYc4130_assertion wasDerivedFrom befree-2016 NP274938.RA5IjPVbERfHRJ2Jp5QlXC-o3R7ihtKN3Fo24KnirjYc4130_provenance.
- NP274938.RA5IjPVbERfHRJ2Jp5QlXC-o3R7ihtKN3Fo24KnirjYc4130_assertion wasGeneratedBy ECO_0000203 NP274938.RA5IjPVbERfHRJ2Jp5QlXC-o3R7ihtKN3Fo24KnirjYc4130_provenance.
- befree-2016 importedOn "2016-02-19" NP274938.RA5IjPVbERfHRJ2Jp5QlXC-o3R7ihtKN3Fo24KnirjYc4130_provenance.