Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP801308.RAN_bVjL9j0OXP7x_zM53Htj2gNwgnSL8tFmtGKLlWccc130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP801308.RAN_bVjL9j0OXP7x_zM53Htj2gNwgnSL8tFmtGKLlWccc130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP801308.RAN_bVjL9j0OXP7x_zM53Htj2gNwgnSL8tFmtGKLlWccc130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP801308.RAN_bVjL9j0OXP7x_zM53Htj2gNwgnSL8tFmtGKLlWccc130_provenance.
- NP801308.RAN_bVjL9j0OXP7x_zM53Htj2gNwgnSL8tFmtGKLlWccc130_assertion description "[Mutations in ALDH4A1 are associated with type II hyperprolinemia.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP801308.RAN_bVjL9j0OXP7x_zM53Htj2gNwgnSL8tFmtGKLlWccc130_provenance.
- NP801308.RAN_bVjL9j0OXP7x_zM53Htj2gNwgnSL8tFmtGKLlWccc130_assertion evidence source_evidence_literature NP801308.RAN_bVjL9j0OXP7x_zM53Htj2gNwgnSL8tFmtGKLlWccc130_provenance.
- NP801308.RAN_bVjL9j0OXP7x_zM53Htj2gNwgnSL8tFmtGKLlWccc130_assertion SIO_000772 10971205 NP801308.RAN_bVjL9j0OXP7x_zM53Htj2gNwgnSL8tFmtGKLlWccc130_provenance.
- NP801308.RAN_bVjL9j0OXP7x_zM53Htj2gNwgnSL8tFmtGKLlWccc130_assertion wasDerivedFrom befree-20150227 NP801308.RAN_bVjL9j0OXP7x_zM53Htj2gNwgnSL8tFmtGKLlWccc130_provenance.
- NP801308.RAN_bVjL9j0OXP7x_zM53Htj2gNwgnSL8tFmtGKLlWccc130_assertion wasGeneratedBy ECO_0000203 NP801308.RAN_bVjL9j0OXP7x_zM53Htj2gNwgnSL8tFmtGKLlWccc130_provenance.
- befree-20150227 importedOn "2015-02-27" NP801308.RAN_bVjL9j0OXP7x_zM53Htj2gNwgnSL8tFmtGKLlWccc130_provenance.