Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP703108.RAotLa3yZKykHGv1XKkEZ2UvDf4Rp2088U_v0DPCFPxcU130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP703108.RAotLa3yZKykHGv1XKkEZ2UvDf4Rp2088U_v0DPCFPxcU130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP703108.RAotLa3yZKykHGv1XKkEZ2UvDf4Rp2088U_v0DPCFPxcU130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP703108.RAotLa3yZKykHGv1XKkEZ2UvDf4Rp2088U_v0DPCFPxcU130_provenance.
- NP703108.RAotLa3yZKykHGv1XKkEZ2UvDf4Rp2088U_v0DPCFPxcU130_assertion description "[We conclude that deletions of hSNF5/INI1 are frequent in patients with CML.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP703108.RAotLa3yZKykHGv1XKkEZ2UvDf4Rp2088U_v0DPCFPxcU130_provenance.
- NP703108.RAotLa3yZKykHGv1XKkEZ2UvDf4Rp2088U_v0DPCFPxcU130_assertion evidence source_evidence_literature NP703108.RAotLa3yZKykHGv1XKkEZ2UvDf4Rp2088U_v0DPCFPxcU130_provenance.
- NP703108.RAotLa3yZKykHGv1XKkEZ2UvDf4Rp2088U_v0DPCFPxcU130_assertion SIO_000772 10463572 NP703108.RAotLa3yZKykHGv1XKkEZ2UvDf4Rp2088U_v0DPCFPxcU130_provenance.
- NP703108.RAotLa3yZKykHGv1XKkEZ2UvDf4Rp2088U_v0DPCFPxcU130_assertion wasDerivedFrom befree-20150227 NP703108.RAotLa3yZKykHGv1XKkEZ2UvDf4Rp2088U_v0DPCFPxcU130_provenance.
- NP703108.RAotLa3yZKykHGv1XKkEZ2UvDf4Rp2088U_v0DPCFPxcU130_assertion wasGeneratedBy ECO_0000203 NP703108.RAotLa3yZKykHGv1XKkEZ2UvDf4Rp2088U_v0DPCFPxcU130_provenance.
- befree-20150227 importedOn "2015-02-27" NP703108.RAotLa3yZKykHGv1XKkEZ2UvDf4Rp2088U_v0DPCFPxcU130_provenance.