Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP447426.RAWg8Z5_nBS6MDxDO6ZXIW-142pUfY-_RyLHbg-WigpQ8130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP447426.RAWg8Z5_nBS6MDxDO6ZXIW-142pUfY-_RyLHbg-WigpQ8130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP447426.RAWg8Z5_nBS6MDxDO6ZXIW-142pUfY-_RyLHbg-WigpQ8130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP447426.RAWg8Z5_nBS6MDxDO6ZXIW-142pUfY-_RyLHbg-WigpQ8130_provenance.
- NP447426.RAWg8Z5_nBS6MDxDO6ZXIW-142pUfY-_RyLHbg-WigpQ8130_assertion description "[Alkaptonuria is caused by a defect in the enzyme homogentisate 1,2-dioxygenase with subsequent accumulation of homogentisic acid.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP447426.RAWg8Z5_nBS6MDxDO6ZXIW-142pUfY-_RyLHbg-WigpQ8130_provenance.
- NP447426.RAWg8Z5_nBS6MDxDO6ZXIW-142pUfY-_RyLHbg-WigpQ8130_assertion evidence source_evidence_literature NP447426.RAWg8Z5_nBS6MDxDO6ZXIW-142pUfY-_RyLHbg-WigpQ8130_provenance.
- NP447426.RAWg8Z5_nBS6MDxDO6ZXIW-142pUfY-_RyLHbg-WigpQ8130_assertion SIO_000772 23632174 NP447426.RAWg8Z5_nBS6MDxDO6ZXIW-142pUfY-_RyLHbg-WigpQ8130_provenance.
- NP447426.RAWg8Z5_nBS6MDxDO6ZXIW-142pUfY-_RyLHbg-WigpQ8130_assertion wasDerivedFrom befree-20150227 NP447426.RAWg8Z5_nBS6MDxDO6ZXIW-142pUfY-_RyLHbg-WigpQ8130_provenance.
- NP447426.RAWg8Z5_nBS6MDxDO6ZXIW-142pUfY-_RyLHbg-WigpQ8130_assertion wasGeneratedBy ECO_0000203 NP447426.RAWg8Z5_nBS6MDxDO6ZXIW-142pUfY-_RyLHbg-WigpQ8130_provenance.
- befree-20150227 importedOn "2015-02-27" NP447426.RAWg8Z5_nBS6MDxDO6ZXIW-142pUfY-_RyLHbg-WigpQ8130_provenance.