Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP6160.RAAYWL0rDW-14U3rWV0BnnXWj-GG1Fzw6yO27x3GxdSNA130_provenance>. }
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- source_evidence_curated type ECO_0000205 NP6160.RAAYWL0rDW-14U3rWV0BnnXWj-GG1Fzw6yO27x3GxdSNA130_provenance.
- source_evidence_curated label "DisGeNET evidence - CURATED" NP6160.RAAYWL0rDW-14U3rWV0BnnXWj-GG1Fzw6yO27x3GxdSNA130_provenance.
- source_evidence_curated comment "Gene-disease associations manually curated." NP6160.RAAYWL0rDW-14U3rWV0BnnXWj-GG1Fzw6yO27x3GxdSNA130_provenance.
- NP6160.RAAYWL0rDW-14U3rWV0BnnXWj-GG1Fzw6yO27x3GxdSNA130_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." NP6160.RAAYWL0rDW-14U3rWV0BnnXWj-GG1Fzw6yO27x3GxdSNA130_provenance.
- NP6160.RAAYWL0rDW-14U3rWV0BnnXWj-GG1Fzw6yO27x3GxdSNA130_assertion evidence source_evidence_curated NP6160.RAAYWL0rDW-14U3rWV0BnnXWj-GG1Fzw6yO27x3GxdSNA130_provenance.
- NP6160.RAAYWL0rDW-14U3rWV0BnnXWj-GG1Fzw6yO27x3GxdSNA130_assertion SIO_000772 17446347 NP6160.RAAYWL0rDW-14U3rWV0BnnXWj-GG1Fzw6yO27x3GxdSNA130_provenance.
- NP6160.RAAYWL0rDW-14U3rWV0BnnXWj-GG1Fzw6yO27x3GxdSNA130_assertion wasDerivedFrom uniprot-20130724 NP6160.RAAYWL0rDW-14U3rWV0BnnXWj-GG1Fzw6yO27x3GxdSNA130_provenance.
- NP6160.RAAYWL0rDW-14U3rWV0BnnXWj-GG1Fzw6yO27x3GxdSNA130_assertion wasGeneratedBy ECO_0000218 NP6160.RAAYWL0rDW-14U3rWV0BnnXWj-GG1Fzw6yO27x3GxdSNA130_provenance.
- uniprot-20130724 importedOn "2013-07-24" NP6160.RAAYWL0rDW-14U3rWV0BnnXWj-GG1Fzw6yO27x3GxdSNA130_provenance.