Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP1294957.RALAJPpWD-a2pQkz65dfJo39sLO6YC4GXdd_B3Kr-Fbyg130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP1294957.RALAJPpWD-a2pQkz65dfJo39sLO6YC4GXdd_B3Kr-Fbyg130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP1294957.RALAJPpWD-a2pQkz65dfJo39sLO6YC4GXdd_B3Kr-Fbyg130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP1294957.RALAJPpWD-a2pQkz65dfJo39sLO6YC4GXdd_B3Kr-Fbyg130_provenance.
- NP1294957.RALAJPpWD-a2pQkz65dfJo39sLO6YC4GXdd_B3Kr-Fbyg130_assertion description "[Although the karyotypic abnormalities and phenotypes were varied, there was a high degree of association between the karyotypic abnormalities monosomy 7/del (7q) and the CD34-positive phenotype; this antigen was expressed on blasts from eight of the nine patients displaying this abnormality.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1294957.RALAJPpWD-a2pQkz65dfJo39sLO6YC4GXdd_B3Kr-Fbyg130_provenance.
- NP1294957.RALAJPpWD-a2pQkz65dfJo39sLO6YC4GXdd_B3Kr-Fbyg130_assertion evidence source_evidence_literature NP1294957.RALAJPpWD-a2pQkz65dfJo39sLO6YC4GXdd_B3Kr-Fbyg130_provenance.
- NP1294957.RALAJPpWD-a2pQkz65dfJo39sLO6YC4GXdd_B3Kr-Fbyg130_assertion SIO_000772 2646903 NP1294957.RALAJPpWD-a2pQkz65dfJo39sLO6YC4GXdd_B3Kr-Fbyg130_provenance.
- NP1294957.RALAJPpWD-a2pQkz65dfJo39sLO6YC4GXdd_B3Kr-Fbyg130_assertion wasDerivedFrom befree-2016 NP1294957.RALAJPpWD-a2pQkz65dfJo39sLO6YC4GXdd_B3Kr-Fbyg130_provenance.
- NP1294957.RALAJPpWD-a2pQkz65dfJo39sLO6YC4GXdd_B3Kr-Fbyg130_assertion wasGeneratedBy ECO_0000203 NP1294957.RALAJPpWD-a2pQkz65dfJo39sLO6YC4GXdd_B3Kr-Fbyg130_provenance.
- befree-2016 importedOn "2016-02-19" NP1294957.RALAJPpWD-a2pQkz65dfJo39sLO6YC4GXdd_B3Kr-Fbyg130_provenance.