Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP354206.RA6LyEaxPtyAwVH7UnCxxURK-ddic9if1Vyn8B86Oy99U130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP354206.RA6LyEaxPtyAwVH7UnCxxURK-ddic9if1Vyn8B86Oy99U130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP354206.RA6LyEaxPtyAwVH7UnCxxURK-ddic9if1Vyn8B86Oy99U130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP354206.RA6LyEaxPtyAwVH7UnCxxURK-ddic9if1Vyn8B86Oy99U130_provenance.
- NP354206.RA6LyEaxPtyAwVH7UnCxxURK-ddic9if1Vyn8B86Oy99U130_assertion description "[Crigler-Najjar syndrome type 1 (CN type 1) is an autosomal recessive disorder characterized by nonhemolytic jaundice resulting from mutations to the gene encoding bilirubin-UDP-glucuronosyltransferase (UDPGT).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP354206.RA6LyEaxPtyAwVH7UnCxxURK-ddic9if1Vyn8B86Oy99U130_provenance.
- NP354206.RA6LyEaxPtyAwVH7UnCxxURK-ddic9if1Vyn8B86Oy99U130_assertion evidence source_evidence_literature NP354206.RA6LyEaxPtyAwVH7UnCxxURK-ddic9if1Vyn8B86Oy99U130_provenance.
- NP354206.RA6LyEaxPtyAwVH7UnCxxURK-ddic9if1Vyn8B86Oy99U130_assertion SIO_000772 9525311 NP354206.RA6LyEaxPtyAwVH7UnCxxURK-ddic9if1Vyn8B86Oy99U130_provenance.
- NP354206.RA6LyEaxPtyAwVH7UnCxxURK-ddic9if1Vyn8B86Oy99U130_assertion wasDerivedFrom befree-20140225 NP354206.RA6LyEaxPtyAwVH7UnCxxURK-ddic9if1Vyn8B86Oy99U130_provenance.
- NP354206.RA6LyEaxPtyAwVH7UnCxxURK-ddic9if1Vyn8B86Oy99U130_assertion wasGeneratedBy ECO_0000203 NP354206.RA6LyEaxPtyAwVH7UnCxxURK-ddic9if1Vyn8B86Oy99U130_provenance.
- befree-20140225 importedOn "2014-02-25" NP354206.RA6LyEaxPtyAwVH7UnCxxURK-ddic9if1Vyn8B86Oy99U130_provenance.