Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP228426.RAVnMof-_8Wc5ksN2DydtQ4VMNN_7JswTicoWSuaXHPxw130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP228426.RAVnMof-_8Wc5ksN2DydtQ4VMNN_7JswTicoWSuaXHPxw130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP228426.RAVnMof-_8Wc5ksN2DydtQ4VMNN_7JswTicoWSuaXHPxw130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP228426.RAVnMof-_8Wc5ksN2DydtQ4VMNN_7JswTicoWSuaXHPxw130_provenance.
- NP228426.RAVnMof-_8Wc5ksN2DydtQ4VMNN_7JswTicoWSuaXHPxw130_assertion description "[The authors also found that LOHs at 1p36, 9p21, and 17p13 may play an important role in Barrett esophagus (BE), LOHs at 10q23, 17p13, and 17q12 in low-grade dysplasia (LGD), LOHs at 5q23 and 17q21 in high-grade dysplasia (HGD), and LOHs at 5q23 and 21q22 in adenocarcinoma.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP228426.RAVnMof-_8Wc5ksN2DydtQ4VMNN_7JswTicoWSuaXHPxw130_provenance.
- NP228426.RAVnMof-_8Wc5ksN2DydtQ4VMNN_7JswTicoWSuaXHPxw130_assertion evidence source_evidence_literature NP228426.RAVnMof-_8Wc5ksN2DydtQ4VMNN_7JswTicoWSuaXHPxw130_provenance.
- NP228426.RAVnMof-_8Wc5ksN2DydtQ4VMNN_7JswTicoWSuaXHPxw130_assertion SIO_000772 19347831 NP228426.RAVnMof-_8Wc5ksN2DydtQ4VMNN_7JswTicoWSuaXHPxw130_provenance.
- NP228426.RAVnMof-_8Wc5ksN2DydtQ4VMNN_7JswTicoWSuaXHPxw130_assertion wasDerivedFrom befree-20140225 NP228426.RAVnMof-_8Wc5ksN2DydtQ4VMNN_7JswTicoWSuaXHPxw130_provenance.
- NP228426.RAVnMof-_8Wc5ksN2DydtQ4VMNN_7JswTicoWSuaXHPxw130_assertion wasGeneratedBy ECO_0000203 NP228426.RAVnMof-_8Wc5ksN2DydtQ4VMNN_7JswTicoWSuaXHPxw130_provenance.
- befree-20140225 importedOn "2014-02-25" NP228426.RAVnMof-_8Wc5ksN2DydtQ4VMNN_7JswTicoWSuaXHPxw130_provenance.