Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP670552.RAD3NKtTM9dgn6ZodHy1Y1RLeLoz5QBlnhfd-QmwFO8os130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP670552.RAD3NKtTM9dgn6ZodHy1Y1RLeLoz5QBlnhfd-QmwFO8os130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP670552.RAD3NKtTM9dgn6ZodHy1Y1RLeLoz5QBlnhfd-QmwFO8os130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP670552.RAD3NKtTM9dgn6ZodHy1Y1RLeLoz5QBlnhfd-QmwFO8os130_provenance.
- NP670552.RAD3NKtTM9dgn6ZodHy1Y1RLeLoz5QBlnhfd-QmwFO8os130_assertion description "[The high frequency of ARDS in patients with MTP defects suggests that this inborn error may be a risk factor for ARDS.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP670552.RAD3NKtTM9dgn6ZodHy1Y1RLeLoz5QBlnhfd-QmwFO8os130_provenance.
- NP670552.RAD3NKtTM9dgn6ZodHy1Y1RLeLoz5QBlnhfd-QmwFO8os130_assertion evidence source_evidence_literature NP670552.RAD3NKtTM9dgn6ZodHy1Y1RLeLoz5QBlnhfd-QmwFO8os130_provenance.
- NP670552.RAD3NKtTM9dgn6ZodHy1Y1RLeLoz5QBlnhfd-QmwFO8os130_assertion SIO_000772 14605499 NP670552.RAD3NKtTM9dgn6ZodHy1Y1RLeLoz5QBlnhfd-QmwFO8os130_provenance.
- NP670552.RAD3NKtTM9dgn6ZodHy1Y1RLeLoz5QBlnhfd-QmwFO8os130_assertion wasDerivedFrom befree-20140225 NP670552.RAD3NKtTM9dgn6ZodHy1Y1RLeLoz5QBlnhfd-QmwFO8os130_provenance.
- NP670552.RAD3NKtTM9dgn6ZodHy1Y1RLeLoz5QBlnhfd-QmwFO8os130_assertion wasGeneratedBy ECO_0000203 NP670552.RAD3NKtTM9dgn6ZodHy1Y1RLeLoz5QBlnhfd-QmwFO8os130_provenance.
- befree-20140225 importedOn "2014-02-25" NP670552.RAD3NKtTM9dgn6ZodHy1Y1RLeLoz5QBlnhfd-QmwFO8os130_provenance.