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- source_evidence_literature type ECO_0000212 NP443211.RABQ46yDf6P3krCaO1-5_0Lpxkd8B4YuLQwfREvMgqZdg130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP443211.RABQ46yDf6P3krCaO1-5_0Lpxkd8B4YuLQwfREvMgqZdg130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP443211.RABQ46yDf6P3krCaO1-5_0Lpxkd8B4YuLQwfREvMgqZdg130_provenance.
- NP443211.RABQ46yDf6P3krCaO1-5_0Lpxkd8B4YuLQwfREvMgqZdg130_assertion description "[Other mutations in HADHA or HADHB often lead to significant reduction in all three enzymatic activities and result in trifunctional protein deficiency (TFPD).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP443211.RABQ46yDf6P3krCaO1-5_0Lpxkd8B4YuLQwfREvMgqZdg130_provenance.
- NP443211.RABQ46yDf6P3krCaO1-5_0Lpxkd8B4YuLQwfREvMgqZdg130_assertion evidence source_evidence_literature NP443211.RABQ46yDf6P3krCaO1-5_0Lpxkd8B4YuLQwfREvMgqZdg130_provenance.
- NP443211.RABQ46yDf6P3krCaO1-5_0Lpxkd8B4YuLQwfREvMgqZdg130_assertion SIO_000772 22459206 NP443211.RABQ46yDf6P3krCaO1-5_0Lpxkd8B4YuLQwfREvMgqZdg130_provenance.
- NP443211.RABQ46yDf6P3krCaO1-5_0Lpxkd8B4YuLQwfREvMgqZdg130_assertion wasDerivedFrom befree-20150227 NP443211.RABQ46yDf6P3krCaO1-5_0Lpxkd8B4YuLQwfREvMgqZdg130_provenance.
- NP443211.RABQ46yDf6P3krCaO1-5_0Lpxkd8B4YuLQwfREvMgqZdg130_assertion wasGeneratedBy ECO_0000203 NP443211.RABQ46yDf6P3krCaO1-5_0Lpxkd8B4YuLQwfREvMgqZdg130_provenance.
- befree-20150227 importedOn "2015-02-27" NP443211.RABQ46yDf6P3krCaO1-5_0Lpxkd8B4YuLQwfREvMgqZdg130_provenance.