Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP838331.RAh3F8rmjPsSiJ2FLg6MbO1MYawBjRFwVB1HStxf0Cax8130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP838331.RAh3F8rmjPsSiJ2FLg6MbO1MYawBjRFwVB1HStxf0Cax8130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP838331.RAh3F8rmjPsSiJ2FLg6MbO1MYawBjRFwVB1HStxf0Cax8130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP838331.RAh3F8rmjPsSiJ2FLg6MbO1MYawBjRFwVB1HStxf0Cax8130_provenance.
- befree-2016 importedOn "2016-02-19" NP838331.RAh3F8rmjPsSiJ2FLg6MbO1MYawBjRFwVB1HStxf0Cax8130_provenance.
- NP838331.RAh3F8rmjPsSiJ2FLg6MbO1MYawBjRFwVB1HStxf0Cax8130_assertion wasGeneratedBy ECO_0000203 NP838331.RAh3F8rmjPsSiJ2FLg6MbO1MYawBjRFwVB1HStxf0Cax8130_provenance.
- NP838331.RAh3F8rmjPsSiJ2FLg6MbO1MYawBjRFwVB1HStxf0Cax8130_assertion wasDerivedFrom befree-2016 NP838331.RAh3F8rmjPsSiJ2FLg6MbO1MYawBjRFwVB1HStxf0Cax8130_provenance.
- NP838331.RAh3F8rmjPsSiJ2FLg6MbO1MYawBjRFwVB1HStxf0Cax8130_assertion SIO_000772 20830319 NP838331.RAh3F8rmjPsSiJ2FLg6MbO1MYawBjRFwVB1HStxf0Cax8130_provenance.
- NP838331.RAh3F8rmjPsSiJ2FLg6MbO1MYawBjRFwVB1HStxf0Cax8130_assertion evidence source_evidence_literature NP838331.RAh3F8rmjPsSiJ2FLg6MbO1MYawBjRFwVB1HStxf0Cax8130_provenance.
- NP838331.RAh3F8rmjPsSiJ2FLg6MbO1MYawBjRFwVB1HStxf0Cax8130_assertion description "[Phenylketonuria (PKU) is characterized by persistent hyperphenylalaninemia, due to mutations in the gene coding for phenylalanine hydroxylase (PAH).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP838331.RAh3F8rmjPsSiJ2FLg6MbO1MYawBjRFwVB1HStxf0Cax8130_provenance.