Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP826853.RAnM_H-HT9YWy9zorSmW3GII1-V58R8p8Ll0Awa5Yi6bU130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP826853.RAnM_H-HT9YWy9zorSmW3GII1-V58R8p8Ll0Awa5Yi6bU130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP826853.RAnM_H-HT9YWy9zorSmW3GII1-V58R8p8Ll0Awa5Yi6bU130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP826853.RAnM_H-HT9YWy9zorSmW3GII1-V58R8p8Ll0Awa5Yi6bU130_provenance.
- NP826853.RAnM_H-HT9YWy9zorSmW3GII1-V58R8p8Ll0Awa5Yi6bU130_assertion description "[Molecular alterations of p73 in human esophageal squamous cell carcinomas: loss of heterozygosity occurs frequently; loss of imprinting and elevation of p73 expression may be related to defective p53.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP826853.RAnM_H-HT9YWy9zorSmW3GII1-V58R8p8Ll0Awa5Yi6bU130_provenance.
- NP826853.RAnM_H-HT9YWy9zorSmW3GII1-V58R8p8Ll0Awa5Yi6bU130_assertion evidence source_evidence_literature NP826853.RAnM_H-HT9YWy9zorSmW3GII1-V58R8p8Ll0Awa5Yi6bU130_provenance.
- NP826853.RAnM_H-HT9YWy9zorSmW3GII1-V58R8p8Ll0Awa5Yi6bU130_assertion SIO_000772 10753204 NP826853.RAnM_H-HT9YWy9zorSmW3GII1-V58R8p8Ll0Awa5Yi6bU130_provenance.
- NP826853.RAnM_H-HT9YWy9zorSmW3GII1-V58R8p8Ll0Awa5Yi6bU130_assertion wasDerivedFrom befree-20140225 NP826853.RAnM_H-HT9YWy9zorSmW3GII1-V58R8p8Ll0Awa5Yi6bU130_provenance.
- NP826853.RAnM_H-HT9YWy9zorSmW3GII1-V58R8p8Ll0Awa5Yi6bU130_assertion wasGeneratedBy ECO_0000203 NP826853.RAnM_H-HT9YWy9zorSmW3GII1-V58R8p8Ll0Awa5Yi6bU130_provenance.
- befree-20140225 importedOn "2014-02-25" NP826853.RAnM_H-HT9YWy9zorSmW3GII1-V58R8p8Ll0Awa5Yi6bU130_provenance.