Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP286409.RAF2Wc-lpGfsvso-eyc3jKIaDARxDRibHjVLumfvK6W_o130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP286409.RAF2Wc-lpGfsvso-eyc3jKIaDARxDRibHjVLumfvK6W_o130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP286409.RAF2Wc-lpGfsvso-eyc3jKIaDARxDRibHjVLumfvK6W_o130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP286409.RAF2Wc-lpGfsvso-eyc3jKIaDARxDRibHjVLumfvK6W_o130_provenance.
- NP286409.RAF2Wc-lpGfsvso-eyc3jKIaDARxDRibHjVLumfvK6W_o130_assertion description "[Holoprosencephaly, sacral anomalies, and situs ambiguus in an infant with partial monosomy 7q/trisomy 2p and SHH and HLXB9 haploinsufficiency..]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP286409.RAF2Wc-lpGfsvso-eyc3jKIaDARxDRibHjVLumfvK6W_o130_provenance.
- NP286409.RAF2Wc-lpGfsvso-eyc3jKIaDARxDRibHjVLumfvK6W_o130_assertion evidence source_evidence_literature NP286409.RAF2Wc-lpGfsvso-eyc3jKIaDARxDRibHjVLumfvK6W_o130_provenance.
- NP286409.RAF2Wc-lpGfsvso-eyc3jKIaDARxDRibHjVLumfvK6W_o130_assertion SIO_000772 10852374 NP286409.RAF2Wc-lpGfsvso-eyc3jKIaDARxDRibHjVLumfvK6W_o130_provenance.
- NP286409.RAF2Wc-lpGfsvso-eyc3jKIaDARxDRibHjVLumfvK6W_o130_assertion wasDerivedFrom befree-2016 NP286409.RAF2Wc-lpGfsvso-eyc3jKIaDARxDRibHjVLumfvK6W_o130_provenance.
- NP286409.RAF2Wc-lpGfsvso-eyc3jKIaDARxDRibHjVLumfvK6W_o130_assertion wasGeneratedBy ECO_0000203 NP286409.RAF2Wc-lpGfsvso-eyc3jKIaDARxDRibHjVLumfvK6W_o130_provenance.
- befree-2016 importedOn "2016-02-19" NP286409.RAF2Wc-lpGfsvso-eyc3jKIaDARxDRibHjVLumfvK6W_o130_provenance.