Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP506755.RAyfEbb28VGbWXQhHIThm6SmEyV67We_pV7PRFKLOgw5s130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP506755.RAyfEbb28VGbWXQhHIThm6SmEyV67We_pV7PRFKLOgw5s130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP506755.RAyfEbb28VGbWXQhHIThm6SmEyV67We_pV7PRFKLOgw5s130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP506755.RAyfEbb28VGbWXQhHIThm6SmEyV67We_pV7PRFKLOgw5s130_provenance.
- NP506755.RAyfEbb28VGbWXQhHIThm6SmEyV67We_pV7PRFKLOgw5s130_assertion description "[Fifteen different mutations of the aldolase B (ALDOB) gene were identified in HFI patients.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP506755.RAyfEbb28VGbWXQhHIThm6SmEyV67We_pV7PRFKLOgw5s130_provenance.
- NP506755.RAyfEbb28VGbWXQhHIThm6SmEyV67We_pV7PRFKLOgw5s130_assertion evidence source_evidence_literature NP506755.RAyfEbb28VGbWXQhHIThm6SmEyV67We_pV7PRFKLOgw5s130_provenance.
- NP506755.RAyfEbb28VGbWXQhHIThm6SmEyV67We_pV7PRFKLOgw5s130_assertion SIO_000772 15880727 NP506755.RAyfEbb28VGbWXQhHIThm6SmEyV67We_pV7PRFKLOgw5s130_provenance.
- NP506755.RAyfEbb28VGbWXQhHIThm6SmEyV67We_pV7PRFKLOgw5s130_assertion wasDerivedFrom befree-20140225 NP506755.RAyfEbb28VGbWXQhHIThm6SmEyV67We_pV7PRFKLOgw5s130_provenance.
- NP506755.RAyfEbb28VGbWXQhHIThm6SmEyV67We_pV7PRFKLOgw5s130_assertion wasGeneratedBy ECO_0000203 NP506755.RAyfEbb28VGbWXQhHIThm6SmEyV67We_pV7PRFKLOgw5s130_provenance.
- befree-20140225 importedOn "2014-02-25" NP506755.RAyfEbb28VGbWXQhHIThm6SmEyV67We_pV7PRFKLOgw5s130_provenance.