Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP1269.RAUN7aJrH2bY7fKIxtkY_uc9hgagVzwOYw1VKGm4ALgsk130_provenance>. }
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- source_evidence_curated type ECO_0000205 NP1269.RAUN7aJrH2bY7fKIxtkY_uc9hgagVzwOYw1VKGm4ALgsk130_provenance.
- source_evidence_curated label "DisGeNET evidence - CURATED" NP1269.RAUN7aJrH2bY7fKIxtkY_uc9hgagVzwOYw1VKGm4ALgsk130_provenance.
- source_evidence_curated comment "Gene-disease associations manually curated." NP1269.RAUN7aJrH2bY7fKIxtkY_uc9hgagVzwOYw1VKGm4ALgsk130_provenance.
- NP1269.RAUN7aJrH2bY7fKIxtkY_uc9hgagVzwOYw1VKGm4ALgsk130_assertion description "[An osteopenic nonfracture syndrome with features of mild osteogenesis imperfecta associated with the substitution of a cysteine for glycine at triple helix position 43 in the pro alpha 1(I) chain of type I collagen.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1269.RAUN7aJrH2bY7fKIxtkY_uc9hgagVzwOYw1VKGm4ALgsk130_provenance.
- NP1269.RAUN7aJrH2bY7fKIxtkY_uc9hgagVzwOYw1VKGm4ALgsk130_assertion evidence source_evidence_curated NP1269.RAUN7aJrH2bY7fKIxtkY_uc9hgagVzwOYw1VKGm4ALgsk130_provenance.
- NP1269.RAUN7aJrH2bY7fKIxtkY_uc9hgagVzwOYw1VKGm4ALgsk130_assertion SIO_000772 1737847 NP1269.RAUN7aJrH2bY7fKIxtkY_uc9hgagVzwOYw1VKGm4ALgsk130_provenance.
- NP1269.RAUN7aJrH2bY7fKIxtkY_uc9hgagVzwOYw1VKGm4ALgsk130_assertion wasDerivedFrom uniprot-20130724 NP1269.RAUN7aJrH2bY7fKIxtkY_uc9hgagVzwOYw1VKGm4ALgsk130_provenance.
- NP1269.RAUN7aJrH2bY7fKIxtkY_uc9hgagVzwOYw1VKGm4ALgsk130_assertion wasGeneratedBy ECO_0000218 NP1269.RAUN7aJrH2bY7fKIxtkY_uc9hgagVzwOYw1VKGm4ALgsk130_provenance.
- uniprot-20130724 importedOn "2013-07-24" NP1269.RAUN7aJrH2bY7fKIxtkY_uc9hgagVzwOYw1VKGm4ALgsk130_provenance.