Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP2177.RA-b2p8-5JCUNRdWQ27v_fjYXAG7LQP9c5R1C8NH-9WDI130_provenance>. }
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- source_evidence_curated type ECO_0000205 NP2177.RA-b2p8-5JCUNRdWQ27v_fjYXAG7LQP9c5R1C8NH-9WDI130_provenance.
- source_evidence_curated label "DisGeNET evidence - CURATED" NP2177.RA-b2p8-5JCUNRdWQ27v_fjYXAG7LQP9c5R1C8NH-9WDI130_provenance.
- source_evidence_curated comment "Gene-disease associations manually curated." NP2177.RA-b2p8-5JCUNRdWQ27v_fjYXAG7LQP9c5R1C8NH-9WDI130_provenance.
- NP2177.RA-b2p8-5JCUNRdWQ27v_fjYXAG7LQP9c5R1C8NH-9WDI130_assertion description "[According to our study, the four mutations account for the majority (88%) of the FANCA alleles in the Israeli Jewish (non-Ashkenazi) FA population.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP2177.RA-b2p8-5JCUNRdWQ27v_fjYXAG7LQP9c5R1C8NH-9WDI130_provenance.
- NP2177.RA-b2p8-5JCUNRdWQ27v_fjYXAG7LQP9c5R1C8NH-9WDI130_assertion evidence source_evidence_curated NP2177.RA-b2p8-5JCUNRdWQ27v_fjYXAG7LQP9c5R1C8NH-9WDI130_provenance.
- NP2177.RA-b2p8-5JCUNRdWQ27v_fjYXAG7LQP9c5R1C8NH-9WDI130_assertion SIO_000772 11091222 NP2177.RA-b2p8-5JCUNRdWQ27v_fjYXAG7LQP9c5R1C8NH-9WDI130_provenance.
- NP2177.RA-b2p8-5JCUNRdWQ27v_fjYXAG7LQP9c5R1C8NH-9WDI130_assertion wasDerivedFrom uniprot-20130724 NP2177.RA-b2p8-5JCUNRdWQ27v_fjYXAG7LQP9c5R1C8NH-9WDI130_provenance.
- NP2177.RA-b2p8-5JCUNRdWQ27v_fjYXAG7LQP9c5R1C8NH-9WDI130_assertion wasGeneratedBy ECO_0000218 NP2177.RA-b2p8-5JCUNRdWQ27v_fjYXAG7LQP9c5R1C8NH-9WDI130_provenance.
- uniprot-20130724 importedOn "2013-07-24" NP2177.RA-b2p8-5JCUNRdWQ27v_fjYXAG7LQP9c5R1C8NH-9WDI130_provenance.