Matches in Nanopublications for { <http://rdf.disgenet.org/nanopublications.trig#NP687755.RABc8AUbewl6m3sWOlJbBXY0Asw5m5vBQyVHFH2_Feg_A130_assertion> ?p ?o ?g. }
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- NP687755.RABc8AUbewl6m3sWOlJbBXY0Asw5m5vBQyVHFH2_Feg_A130_assertion type Assertion NP687755.RABc8AUbewl6m3sWOlJbBXY0Asw5m5vBQyVHFH2_Feg_A130_head.
- NP687755.RABc8AUbewl6m3sWOlJbBXY0Asw5m5vBQyVHFH2_Feg_A130_assertion description "[Hirschsprung disease (HSCR), a developmental disorder characterized by the absence of enteric neurons in distal segments of the gut, shows a complex pattern of inheritance, with the RET protooncogene acting as a major gene and additional susceptibility loci playing minor roles.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP687755.RABc8AUbewl6m3sWOlJbBXY0Asw5m5vBQyVHFH2_Feg_A130_provenance.
- NP687755.RABc8AUbewl6m3sWOlJbBXY0Asw5m5vBQyVHFH2_Feg_A130_assertion evidence source_evidence_literature NP687755.RABc8AUbewl6m3sWOlJbBXY0Asw5m5vBQyVHFH2_Feg_A130_provenance.
- NP687755.RABc8AUbewl6m3sWOlJbBXY0Asw5m5vBQyVHFH2_Feg_A130_assertion SIO_000772 16986122 NP687755.RABc8AUbewl6m3sWOlJbBXY0Asw5m5vBQyVHFH2_Feg_A130_provenance.
- NP687755.RABc8AUbewl6m3sWOlJbBXY0Asw5m5vBQyVHFH2_Feg_A130_assertion wasDerivedFrom befree-20140225 NP687755.RABc8AUbewl6m3sWOlJbBXY0Asw5m5vBQyVHFH2_Feg_A130_provenance.
- NP687755.RABc8AUbewl6m3sWOlJbBXY0Asw5m5vBQyVHFH2_Feg_A130_assertion wasGeneratedBy ECO_0000203 NP687755.RABc8AUbewl6m3sWOlJbBXY0Asw5m5vBQyVHFH2_Feg_A130_provenance.