Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP394582.RAP7slDBK7JG2Bes0VoS4xLHYdZwEn_DQGVwkn-I-CQww130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP394582.RAP7slDBK7JG2Bes0VoS4xLHYdZwEn_DQGVwkn-I-CQww130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP394582.RAP7slDBK7JG2Bes0VoS4xLHYdZwEn_DQGVwkn-I-CQww130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP394582.RAP7slDBK7JG2Bes0VoS4xLHYdZwEn_DQGVwkn-I-CQww130_provenance.
- NP394582.RAP7slDBK7JG2Bes0VoS4xLHYdZwEn_DQGVwkn-I-CQww130_assertion description "[FANCG is one of Fanconi anemia susceptibility genes that participate in DSB repair pathway to prevent chromosomal aberrations.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP394582.RAP7slDBK7JG2Bes0VoS4xLHYdZwEn_DQGVwkn-I-CQww130_provenance.
- NP394582.RAP7slDBK7JG2Bes0VoS4xLHYdZwEn_DQGVwkn-I-CQww130_assertion evidence source_evidence_literature NP394582.RAP7slDBK7JG2Bes0VoS4xLHYdZwEn_DQGVwkn-I-CQww130_provenance.
- NP394582.RAP7slDBK7JG2Bes0VoS4xLHYdZwEn_DQGVwkn-I-CQww130_assertion SIO_000772 21750350 NP394582.RAP7slDBK7JG2Bes0VoS4xLHYdZwEn_DQGVwkn-I-CQww130_provenance.
- NP394582.RAP7slDBK7JG2Bes0VoS4xLHYdZwEn_DQGVwkn-I-CQww130_assertion wasDerivedFrom befree-20150227 NP394582.RAP7slDBK7JG2Bes0VoS4xLHYdZwEn_DQGVwkn-I-CQww130_provenance.
- NP394582.RAP7slDBK7JG2Bes0VoS4xLHYdZwEn_DQGVwkn-I-CQww130_assertion wasGeneratedBy ECO_0000203 NP394582.RAP7slDBK7JG2Bes0VoS4xLHYdZwEn_DQGVwkn-I-CQww130_provenance.
- befree-20150227 importedOn "2015-02-27" NP394582.RAP7slDBK7JG2Bes0VoS4xLHYdZwEn_DQGVwkn-I-CQww130_provenance.