Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP474455.RABj_LHo9nfaWO-bOsUEbUJLtU7qV1tq6LxEK8mNYexrM130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP474455.RABj_LHo9nfaWO-bOsUEbUJLtU7qV1tq6LxEK8mNYexrM130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP474455.RABj_LHo9nfaWO-bOsUEbUJLtU7qV1tq6LxEK8mNYexrM130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP474455.RABj_LHo9nfaWO-bOsUEbUJLtU7qV1tq6LxEK8mNYexrM130_provenance.
- NP474455.RABj_LHo9nfaWO-bOsUEbUJLtU7qV1tq6LxEK8mNYexrM130_assertion description "[TSP-5 is of interest because mutations in the gene cause two skeletal dysplasias, pseudoachondroplasia (PSACH) and multiple epiphyseal dysplasia (MED/EDM1).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP474455.RABj_LHo9nfaWO-bOsUEbUJLtU7qV1tq6LxEK8mNYexrM130_provenance.
- NP474455.RABj_LHo9nfaWO-bOsUEbUJLtU7qV1tq6LxEK8mNYexrM130_assertion evidence source_evidence_literature NP474455.RABj_LHo9nfaWO-bOsUEbUJLtU7qV1tq6LxEK8mNYexrM130_provenance.
- NP474455.RABj_LHo9nfaWO-bOsUEbUJLtU7qV1tq6LxEK8mNYexrM130_assertion SIO_000772 18193163 NP474455.RABj_LHo9nfaWO-bOsUEbUJLtU7qV1tq6LxEK8mNYexrM130_provenance.
- NP474455.RABj_LHo9nfaWO-bOsUEbUJLtU7qV1tq6LxEK8mNYexrM130_assertion wasDerivedFrom befree-20140225 NP474455.RABj_LHo9nfaWO-bOsUEbUJLtU7qV1tq6LxEK8mNYexrM130_provenance.
- NP474455.RABj_LHo9nfaWO-bOsUEbUJLtU7qV1tq6LxEK8mNYexrM130_assertion wasGeneratedBy ECO_0000203 NP474455.RABj_LHo9nfaWO-bOsUEbUJLtU7qV1tq6LxEK8mNYexrM130_provenance.
- befree-20140225 importedOn "2014-02-25" NP474455.RABj_LHo9nfaWO-bOsUEbUJLtU7qV1tq6LxEK8mNYexrM130_provenance.