Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP557365.RA_h3-G722mkTvTSyVFK5weIDHbTsD3e6Py2sltKzY_3Q130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP557365.RA_h3-G722mkTvTSyVFK5weIDHbTsD3e6Py2sltKzY_3Q130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP557365.RA_h3-G722mkTvTSyVFK5weIDHbTsD3e6Py2sltKzY_3Q130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP557365.RA_h3-G722mkTvTSyVFK5weIDHbTsD3e6Py2sltKzY_3Q130_provenance.
- NP557365.RA_h3-G722mkTvTSyVFK5weIDHbTsD3e6Py2sltKzY_3Q130_assertion wasGeneratedBy ECO_0000203 NP557365.RA_h3-G722mkTvTSyVFK5weIDHbTsD3e6Py2sltKzY_3Q130_provenance.
- NP557365.RA_h3-G722mkTvTSyVFK5weIDHbTsD3e6Py2sltKzY_3Q130_assertion wasDerivedFrom befree-20140225 NP557365.RA_h3-G722mkTvTSyVFK5weIDHbTsD3e6Py2sltKzY_3Q130_provenance.
- NP557365.RA_h3-G722mkTvTSyVFK5weIDHbTsD3e6Py2sltKzY_3Q130_assertion SIO_000772 20830319 NP557365.RA_h3-G722mkTvTSyVFK5weIDHbTsD3e6Py2sltKzY_3Q130_provenance.
- NP557365.RA_h3-G722mkTvTSyVFK5weIDHbTsD3e6Py2sltKzY_3Q130_assertion evidence source_evidence_literature NP557365.RA_h3-G722mkTvTSyVFK5weIDHbTsD3e6Py2sltKzY_3Q130_provenance.
- NP557365.RA_h3-G722mkTvTSyVFK5weIDHbTsD3e6Py2sltKzY_3Q130_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." NP557365.RA_h3-G722mkTvTSyVFK5weIDHbTsD3e6Py2sltKzY_3Q130_provenance.
- befree-20140225 importedOn "2014-02-25" NP557365.RA_h3-G722mkTvTSyVFK5weIDHbTsD3e6Py2sltKzY_3Q130_provenance.