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- source_evidence_literature type ECO_0000212 NP1042988.RAd3shWUJx7Tn9biw2sFnj0-byFUU1rkjaB94mf4Tmaxg130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP1042988.RAd3shWUJx7Tn9biw2sFnj0-byFUU1rkjaB94mf4Tmaxg130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP1042988.RAd3shWUJx7Tn9biw2sFnj0-byFUU1rkjaB94mf4Tmaxg130_provenance.
- NP1042988.RAd3shWUJx7Tn9biw2sFnj0-byFUU1rkjaB94mf4Tmaxg130_assertion description "[In summary, we conclude that genetic variations in UBQLN2 and PFN1 in a predominantly Flanders-Belgian cohort of FTLD and ALS patients are extremely rare.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1042988.RAd3shWUJx7Tn9biw2sFnj0-byFUU1rkjaB94mf4Tmaxg130_provenance.
- NP1042988.RAd3shWUJx7Tn9biw2sFnj0-byFUU1rkjaB94mf4Tmaxg130_assertion evidence source_evidence_literature NP1042988.RAd3shWUJx7Tn9biw2sFnj0-byFUU1rkjaB94mf4Tmaxg130_provenance.
- NP1042988.RAd3shWUJx7Tn9biw2sFnj0-byFUU1rkjaB94mf4Tmaxg130_assertion SIO_000772 23312802 NP1042988.RAd3shWUJx7Tn9biw2sFnj0-byFUU1rkjaB94mf4Tmaxg130_provenance.
- NP1042988.RAd3shWUJx7Tn9biw2sFnj0-byFUU1rkjaB94mf4Tmaxg130_assertion wasDerivedFrom befree-2016 NP1042988.RAd3shWUJx7Tn9biw2sFnj0-byFUU1rkjaB94mf4Tmaxg130_provenance.
- NP1042988.RAd3shWUJx7Tn9biw2sFnj0-byFUU1rkjaB94mf4Tmaxg130_assertion wasGeneratedBy ECO_0000203 NP1042988.RAd3shWUJx7Tn9biw2sFnj0-byFUU1rkjaB94mf4Tmaxg130_provenance.
- befree-2016 importedOn "2016-02-19" NP1042988.RAd3shWUJx7Tn9biw2sFnj0-byFUU1rkjaB94mf4Tmaxg130_provenance.