Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP4967.RAgWX-Uf6lGg539QY5Ulmi3p9lWdEjgV9zrCPK44qPsCs130_provenance>. }
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- source_evidence_curated type ECO_0000205 NP4967.RAgWX-Uf6lGg539QY5Ulmi3p9lWdEjgV9zrCPK44qPsCs130_provenance.
- source_evidence_curated label "DisGeNET evidence - CURATED" NP4967.RAgWX-Uf6lGg539QY5Ulmi3p9lWdEjgV9zrCPK44qPsCs130_provenance.
- source_evidence_curated comment "Gene-disease associations manually curated." NP4967.RAgWX-Uf6lGg539QY5Ulmi3p9lWdEjgV9zrCPK44qPsCs130_provenance.
- NP4967.RAgWX-Uf6lGg539QY5Ulmi3p9lWdEjgV9zrCPK44qPsCs130_assertion description "[The spectrum of mutations in the PCFT gene, coding for an intestinal folate transporter, that are the basis for hereditary folate malabsorption.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP4967.RAgWX-Uf6lGg539QY5Ulmi3p9lWdEjgV9zrCPK44qPsCs130_provenance.
- NP4967.RAgWX-Uf6lGg539QY5Ulmi3p9lWdEjgV9zrCPK44qPsCs130_assertion evidence source_evidence_curated NP4967.RAgWX-Uf6lGg539QY5Ulmi3p9lWdEjgV9zrCPK44qPsCs130_provenance.
- NP4967.RAgWX-Uf6lGg539QY5Ulmi3p9lWdEjgV9zrCPK44qPsCs130_assertion SIO_000772 17446347 NP4967.RAgWX-Uf6lGg539QY5Ulmi3p9lWdEjgV9zrCPK44qPsCs130_provenance.
- NP4967.RAgWX-Uf6lGg539QY5Ulmi3p9lWdEjgV9zrCPK44qPsCs130_assertion wasDerivedFrom uniprot-2016 NP4967.RAgWX-Uf6lGg539QY5Ulmi3p9lWdEjgV9zrCPK44qPsCs130_provenance.
- NP4967.RAgWX-Uf6lGg539QY5Ulmi3p9lWdEjgV9zrCPK44qPsCs130_assertion wasGeneratedBy ECO_0000218 NP4967.RAgWX-Uf6lGg539QY5Ulmi3p9lWdEjgV9zrCPK44qPsCs130_provenance.
- uniprot-2016 importedOn "2016-01-25" NP4967.RAgWX-Uf6lGg539QY5Ulmi3p9lWdEjgV9zrCPK44qPsCs130_provenance.