Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP735034.RAiSmA8ufGr4R-sZwIKgM5TYmj1P6oyj0cUBKCApTD9dg130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP735034.RAiSmA8ufGr4R-sZwIKgM5TYmj1P6oyj0cUBKCApTD9dg130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP735034.RAiSmA8ufGr4R-sZwIKgM5TYmj1P6oyj0cUBKCApTD9dg130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP735034.RAiSmA8ufGr4R-sZwIKgM5TYmj1P6oyj0cUBKCApTD9dg130_provenance.
- NP735034.RAiSmA8ufGr4R-sZwIKgM5TYmj1P6oyj0cUBKCApTD9dg130_assertion description "[The cause of neonatal hyperbilirubinemia could not be identified in 64 infants (70.3%), ABO blood group incompatibility in 14.3% and Glucose-6-phosphate dehydrogenase (G-6-PD) deficiency in 8.8%.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP735034.RAiSmA8ufGr4R-sZwIKgM5TYmj1P6oyj0cUBKCApTD9dg130_provenance.
- NP735034.RAiSmA8ufGr4R-sZwIKgM5TYmj1P6oyj0cUBKCApTD9dg130_assertion evidence source_evidence_literature NP735034.RAiSmA8ufGr4R-sZwIKgM5TYmj1P6oyj0cUBKCApTD9dg130_provenance.
- NP735034.RAiSmA8ufGr4R-sZwIKgM5TYmj1P6oyj0cUBKCApTD9dg130_assertion SIO_000772 19397531 NP735034.RAiSmA8ufGr4R-sZwIKgM5TYmj1P6oyj0cUBKCApTD9dg130_provenance.
- NP735034.RAiSmA8ufGr4R-sZwIKgM5TYmj1P6oyj0cUBKCApTD9dg130_assertion wasDerivedFrom befree-2016 NP735034.RAiSmA8ufGr4R-sZwIKgM5TYmj1P6oyj0cUBKCApTD9dg130_provenance.
- NP735034.RAiSmA8ufGr4R-sZwIKgM5TYmj1P6oyj0cUBKCApTD9dg130_assertion wasGeneratedBy ECO_0000203 NP735034.RAiSmA8ufGr4R-sZwIKgM5TYmj1P6oyj0cUBKCApTD9dg130_provenance.
- befree-2016 importedOn "2016-02-19" NP735034.RAiSmA8ufGr4R-sZwIKgM5TYmj1P6oyj0cUBKCApTD9dg130_provenance.