Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP785060.RAkwNnnXQ_ipr_v_HMEeOitxUeDscaphBlEnGFvmxNv6c130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP785060.RAkwNnnXQ_ipr_v_HMEeOitxUeDscaphBlEnGFvmxNv6c130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP785060.RAkwNnnXQ_ipr_v_HMEeOitxUeDscaphBlEnGFvmxNv6c130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP785060.RAkwNnnXQ_ipr_v_HMEeOitxUeDscaphBlEnGFvmxNv6c130_provenance.
- NP785060.RAkwNnnXQ_ipr_v_HMEeOitxUeDscaphBlEnGFvmxNv6c130_assertion description "[p53 mutation was detected in 11 of 45 LMS cases (24%).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP785060.RAkwNnnXQ_ipr_v_HMEeOitxUeDscaphBlEnGFvmxNv6c130_provenance.
- NP785060.RAkwNnnXQ_ipr_v_HMEeOitxUeDscaphBlEnGFvmxNv6c130_assertion evidence source_evidence_literature NP785060.RAkwNnnXQ_ipr_v_HMEeOitxUeDscaphBlEnGFvmxNv6c130_provenance.
- NP785060.RAkwNnnXQ_ipr_v_HMEeOitxUeDscaphBlEnGFvmxNv6c130_assertion SIO_000772 15492995 NP785060.RAkwNnnXQ_ipr_v_HMEeOitxUeDscaphBlEnGFvmxNv6c130_provenance.
- NP785060.RAkwNnnXQ_ipr_v_HMEeOitxUeDscaphBlEnGFvmxNv6c130_assertion wasDerivedFrom befree-20140225 NP785060.RAkwNnnXQ_ipr_v_HMEeOitxUeDscaphBlEnGFvmxNv6c130_provenance.
- NP785060.RAkwNnnXQ_ipr_v_HMEeOitxUeDscaphBlEnGFvmxNv6c130_assertion wasGeneratedBy ECO_0000203 NP785060.RAkwNnnXQ_ipr_v_HMEeOitxUeDscaphBlEnGFvmxNv6c130_provenance.
- befree-20140225 importedOn "2014-02-25" NP785060.RAkwNnnXQ_ipr_v_HMEeOitxUeDscaphBlEnGFvmxNv6c130_provenance.