Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP663900.RAIgmai_KMQ_NbbF2_PB7_8qDQ0ykgb-KuQ89YrpD1kxo130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP663900.RAIgmai_KMQ_NbbF2_PB7_8qDQ0ykgb-KuQ89YrpD1kxo130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP663900.RAIgmai_KMQ_NbbF2_PB7_8qDQ0ykgb-KuQ89YrpD1kxo130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP663900.RAIgmai_KMQ_NbbF2_PB7_8qDQ0ykgb-KuQ89YrpD1kxo130_provenance.
- NP663900.RAIgmai_KMQ_NbbF2_PB7_8qDQ0ykgb-KuQ89YrpD1kxo130_assertion description "[Mutation of the RAD51C gene in a Fanconi anemia-like disorder.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP663900.RAIgmai_KMQ_NbbF2_PB7_8qDQ0ykgb-KuQ89YrpD1kxo130_provenance.
- NP663900.RAIgmai_KMQ_NbbF2_PB7_8qDQ0ykgb-KuQ89YrpD1kxo130_assertion evidence source_evidence_literature NP663900.RAIgmai_KMQ_NbbF2_PB7_8qDQ0ykgb-KuQ89YrpD1kxo130_provenance.
- NP663900.RAIgmai_KMQ_NbbF2_PB7_8qDQ0ykgb-KuQ89YrpD1kxo130_assertion SIO_000772 20400963 NP663900.RAIgmai_KMQ_NbbF2_PB7_8qDQ0ykgb-KuQ89YrpD1kxo130_provenance.
- NP663900.RAIgmai_KMQ_NbbF2_PB7_8qDQ0ykgb-KuQ89YrpD1kxo130_assertion wasDerivedFrom befree-20150227 NP663900.RAIgmai_KMQ_NbbF2_PB7_8qDQ0ykgb-KuQ89YrpD1kxo130_provenance.
- NP663900.RAIgmai_KMQ_NbbF2_PB7_8qDQ0ykgb-KuQ89YrpD1kxo130_assertion wasGeneratedBy ECO_0000203 NP663900.RAIgmai_KMQ_NbbF2_PB7_8qDQ0ykgb-KuQ89YrpD1kxo130_provenance.
- befree-20150227 importedOn "2015-02-27" NP663900.RAIgmai_KMQ_NbbF2_PB7_8qDQ0ykgb-KuQ89YrpD1kxo130_provenance.