Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP290847.RANxTTaWUCi-NWPx4spdLCQ0ZaOXlf6PVV7VtuRuy03HU130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP290847.RANxTTaWUCi-NWPx4spdLCQ0ZaOXlf6PVV7VtuRuy03HU130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP290847.RANxTTaWUCi-NWPx4spdLCQ0ZaOXlf6PVV7VtuRuy03HU130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP290847.RANxTTaWUCi-NWPx4spdLCQ0ZaOXlf6PVV7VtuRuy03HU130_provenance.
- NP290847.RANxTTaWUCi-NWPx4spdLCQ0ZaOXlf6PVV7VtuRuy03HU130_assertion description "[The cblD gene was localized to human chromosome 2q23.2, and a candidate gene, designated MMADHC (methylmalonic aciduria, cblD type, and homocystinuria), was identified in this region.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP290847.RANxTTaWUCi-NWPx4spdLCQ0ZaOXlf6PVV7VtuRuy03HU130_provenance.
- NP290847.RANxTTaWUCi-NWPx4spdLCQ0ZaOXlf6PVV7VtuRuy03HU130_assertion evidence source_evidence_literature NP290847.RANxTTaWUCi-NWPx4spdLCQ0ZaOXlf6PVV7VtuRuy03HU130_provenance.
- NP290847.RANxTTaWUCi-NWPx4spdLCQ0ZaOXlf6PVV7VtuRuy03HU130_assertion SIO_000772 18385497 NP290847.RANxTTaWUCi-NWPx4spdLCQ0ZaOXlf6PVV7VtuRuy03HU130_provenance.
- NP290847.RANxTTaWUCi-NWPx4spdLCQ0ZaOXlf6PVV7VtuRuy03HU130_assertion wasDerivedFrom befree-20140225 NP290847.RANxTTaWUCi-NWPx4spdLCQ0ZaOXlf6PVV7VtuRuy03HU130_provenance.
- NP290847.RANxTTaWUCi-NWPx4spdLCQ0ZaOXlf6PVV7VtuRuy03HU130_assertion wasGeneratedBy ECO_0000203 NP290847.RANxTTaWUCi-NWPx4spdLCQ0ZaOXlf6PVV7VtuRuy03HU130_provenance.
- befree-20140225 importedOn "2014-02-25" NP290847.RANxTTaWUCi-NWPx4spdLCQ0ZaOXlf6PVV7VtuRuy03HU130_provenance.