Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP933012.RARDVNyNWzBFuOwzMG61Y2qO7esfzzWcDtoOKfX8hECEo130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP933012.RARDVNyNWzBFuOwzMG61Y2qO7esfzzWcDtoOKfX8hECEo130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP933012.RARDVNyNWzBFuOwzMG61Y2qO7esfzzWcDtoOKfX8hECEo130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP933012.RARDVNyNWzBFuOwzMG61Y2qO7esfzzWcDtoOKfX8hECEo130_provenance.
- NP933012.RARDVNyNWzBFuOwzMG61Y2qO7esfzzWcDtoOKfX8hECEo130_assertion description "[A human subject homozygous for a deleterious mutation in LMF1 also shows combined lipase deficiency with concomitant hypertriglyceridemia and associated disorders.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP933012.RARDVNyNWzBFuOwzMG61Y2qO7esfzzWcDtoOKfX8hECEo130_provenance.
- NP933012.RARDVNyNWzBFuOwzMG61Y2qO7esfzzWcDtoOKfX8hECEo130_assertion evidence source_evidence_literature NP933012.RARDVNyNWzBFuOwzMG61Y2qO7esfzzWcDtoOKfX8hECEo130_provenance.
- NP933012.RARDVNyNWzBFuOwzMG61Y2qO7esfzzWcDtoOKfX8hECEo130_assertion SIO_000772 17994020 NP933012.RARDVNyNWzBFuOwzMG61Y2qO7esfzzWcDtoOKfX8hECEo130_provenance.
- NP933012.RARDVNyNWzBFuOwzMG61Y2qO7esfzzWcDtoOKfX8hECEo130_assertion wasDerivedFrom befree-20140225 NP933012.RARDVNyNWzBFuOwzMG61Y2qO7esfzzWcDtoOKfX8hECEo130_provenance.
- NP933012.RARDVNyNWzBFuOwzMG61Y2qO7esfzzWcDtoOKfX8hECEo130_assertion wasGeneratedBy ECO_0000203 NP933012.RARDVNyNWzBFuOwzMG61Y2qO7esfzzWcDtoOKfX8hECEo130_provenance.
- befree-20140225 importedOn "2014-02-25" NP933012.RARDVNyNWzBFuOwzMG61Y2qO7esfzzWcDtoOKfX8hECEo130_provenance.