Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP589529.RAXT1VHnTP0i1JH1wnTA4NLJwgfgb4hu3T9w_dkoRJYAM130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP589529.RAXT1VHnTP0i1JH1wnTA4NLJwgfgb4hu3T9w_dkoRJYAM130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP589529.RAXT1VHnTP0i1JH1wnTA4NLJwgfgb4hu3T9w_dkoRJYAM130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP589529.RAXT1VHnTP0i1JH1wnTA4NLJwgfgb4hu3T9w_dkoRJYAM130_provenance.
- NP589529.RAXT1VHnTP0i1JH1wnTA4NLJwgfgb4hu3T9w_dkoRJYAM130_assertion description "[We found new recurrent alterations in four genes (ARID1A, RPS6KA3, NFE2L2 and IRF2) not previously described in HCC.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP589529.RAXT1VHnTP0i1JH1wnTA4NLJwgfgb4hu3T9w_dkoRJYAM130_provenance.
- NP589529.RAXT1VHnTP0i1JH1wnTA4NLJwgfgb4hu3T9w_dkoRJYAM130_assertion evidence source_evidence_literature NP589529.RAXT1VHnTP0i1JH1wnTA4NLJwgfgb4hu3T9w_dkoRJYAM130_provenance.
- NP589529.RAXT1VHnTP0i1JH1wnTA4NLJwgfgb4hu3T9w_dkoRJYAM130_assertion SIO_000772 22561517 NP589529.RAXT1VHnTP0i1JH1wnTA4NLJwgfgb4hu3T9w_dkoRJYAM130_provenance.
- NP589529.RAXT1VHnTP0i1JH1wnTA4NLJwgfgb4hu3T9w_dkoRJYAM130_assertion wasDerivedFrom befree-20150227 NP589529.RAXT1VHnTP0i1JH1wnTA4NLJwgfgb4hu3T9w_dkoRJYAM130_provenance.
- NP589529.RAXT1VHnTP0i1JH1wnTA4NLJwgfgb4hu3T9w_dkoRJYAM130_assertion wasGeneratedBy ECO_0000203 NP589529.RAXT1VHnTP0i1JH1wnTA4NLJwgfgb4hu3T9w_dkoRJYAM130_provenance.
- befree-20150227 importedOn "2015-02-27" NP589529.RAXT1VHnTP0i1JH1wnTA4NLJwgfgb4hu3T9w_dkoRJYAM130_provenance.