Matches in Nanopublications for { <http://rdf.disgenet.org/nanopublications.trig#NP474455.RABj_LHo9nfaWO-bOsUEbUJLtU7qV1tq6LxEK8mNYexrM130_assertion> ?p ?o ?g. }
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- NP474455.RABj_LHo9nfaWO-bOsUEbUJLtU7qV1tq6LxEK8mNYexrM130_assertion type Assertion NP474455.RABj_LHo9nfaWO-bOsUEbUJLtU7qV1tq6LxEK8mNYexrM130_head.
- 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.