Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP56834.RAI1JZ3bUoPaxe_ML0y4kt6PnA83ID0gmWo-nePEkhFCU130_assertion> ?p ?o ?g. }
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- NP56834.RAI1JZ3bUoPaxe_ML0y4kt6PnA83ID0gmWo-nePEkhFCU130_assertion type Assertion NP56834.RAI1JZ3bUoPaxe_ML0y4kt6PnA83ID0gmWo-nePEkhFCU130_head.
- NP56834.RAI1JZ3bUoPaxe_ML0y4kt6PnA83ID0gmWo-nePEkhFCU130_assertion description "[Using this approach, possible associations of sequence variation, and hence of variation in DNA repair, with disease risk can be assessed.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP56834.RAI1JZ3bUoPaxe_ML0y4kt6PnA83ID0gmWo-nePEkhFCU130_provenance.
- NP56834.RAI1JZ3bUoPaxe_ML0y4kt6PnA83ID0gmWo-nePEkhFCU130_assertion evidence source_evidence_literature NP56834.RAI1JZ3bUoPaxe_ML0y4kt6PnA83ID0gmWo-nePEkhFCU130_provenance.
- NP56834.RAI1JZ3bUoPaxe_ML0y4kt6PnA83ID0gmWo-nePEkhFCU130_assertion SIO_000772 11062157 NP56834.RAI1JZ3bUoPaxe_ML0y4kt6PnA83ID0gmWo-nePEkhFCU130_provenance.
- NP56834.RAI1JZ3bUoPaxe_ML0y4kt6PnA83ID0gmWo-nePEkhFCU130_assertion wasDerivedFrom gad-20150221 NP56834.RAI1JZ3bUoPaxe_ML0y4kt6PnA83ID0gmWo-nePEkhFCU130_provenance.
- NP56834.RAI1JZ3bUoPaxe_ML0y4kt6PnA83ID0gmWo-nePEkhFCU130_assertion wasGeneratedBy ECO_0000203 NP56834.RAI1JZ3bUoPaxe_ML0y4kt6PnA83ID0gmWo-nePEkhFCU130_provenance.