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- source_evidence_literature type ECO_0000212 NP838329.RA-YO6t0Et_TMWH5bzdBPo6HahNVokiJauCM0m9qxGfhk130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP838329.RA-YO6t0Et_TMWH5bzdBPo6HahNVokiJauCM0m9qxGfhk130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP838329.RA-YO6t0Et_TMWH5bzdBPo6HahNVokiJauCM0m9qxGfhk130_provenance.
- befree-2016 importedOn "2016-02-19" NP838329.RA-YO6t0Et_TMWH5bzdBPo6HahNVokiJauCM0m9qxGfhk130_provenance.
- NP838329.RA-YO6t0Et_TMWH5bzdBPo6HahNVokiJauCM0m9qxGfhk130_assertion wasGeneratedBy ECO_0000203 NP838329.RA-YO6t0Et_TMWH5bzdBPo6HahNVokiJauCM0m9qxGfhk130_provenance.
- NP838329.RA-YO6t0Et_TMWH5bzdBPo6HahNVokiJauCM0m9qxGfhk130_assertion wasDerivedFrom befree-2016 NP838329.RA-YO6t0Et_TMWH5bzdBPo6HahNVokiJauCM0m9qxGfhk130_provenance.
- NP838329.RA-YO6t0Et_TMWH5bzdBPo6HahNVokiJauCM0m9qxGfhk130_assertion SIO_000772 20830319 NP838329.RA-YO6t0Et_TMWH5bzdBPo6HahNVokiJauCM0m9qxGfhk130_provenance.
- NP838329.RA-YO6t0Et_TMWH5bzdBPo6HahNVokiJauCM0m9qxGfhk130_assertion evidence source_evidence_literature NP838329.RA-YO6t0Et_TMWH5bzdBPo6HahNVokiJauCM0m9qxGfhk130_provenance.
- NP838329.RA-YO6t0Et_TMWH5bzdBPo6HahNVokiJauCM0m9qxGfhk130_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." NP838329.RA-YO6t0Et_TMWH5bzdBPo6HahNVokiJauCM0m9qxGfhk130_provenance.