Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP785920.RAck5XKxXTiJpOjq-afEe1rkdz8MlN6WrOReybpqW7U_I130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP785920.RAck5XKxXTiJpOjq-afEe1rkdz8MlN6WrOReybpqW7U_I130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP785920.RAck5XKxXTiJpOjq-afEe1rkdz8MlN6WrOReybpqW7U_I130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP785920.RAck5XKxXTiJpOjq-afEe1rkdz8MlN6WrOReybpqW7U_I130_provenance.
- NP785920.RAck5XKxXTiJpOjq-afEe1rkdz8MlN6WrOReybpqW7U_I130_assertion description "[WISP3 gene mutations are associated with progressive pseudorheumatoid dysplasia (PPD, OMIM208230), an autosomal recessive genetic disease that is characterized by the swelling of multiple joints and disproportionate dwarfism.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP785920.RAck5XKxXTiJpOjq-afEe1rkdz8MlN6WrOReybpqW7U_I130_provenance.
- NP785920.RAck5XKxXTiJpOjq-afEe1rkdz8MlN6WrOReybpqW7U_I130_assertion evidence source_evidence_literature NP785920.RAck5XKxXTiJpOjq-afEe1rkdz8MlN6WrOReybpqW7U_I130_provenance.
- NP785920.RAck5XKxXTiJpOjq-afEe1rkdz8MlN6WrOReybpqW7U_I130_assertion SIO_000772 22685593 NP785920.RAck5XKxXTiJpOjq-afEe1rkdz8MlN6WrOReybpqW7U_I130_provenance.
- NP785920.RAck5XKxXTiJpOjq-afEe1rkdz8MlN6WrOReybpqW7U_I130_assertion wasDerivedFrom befree-20140225 NP785920.RAck5XKxXTiJpOjq-afEe1rkdz8MlN6WrOReybpqW7U_I130_provenance.
- NP785920.RAck5XKxXTiJpOjq-afEe1rkdz8MlN6WrOReybpqW7U_I130_assertion wasGeneratedBy ECO_0000203 NP785920.RAck5XKxXTiJpOjq-afEe1rkdz8MlN6WrOReybpqW7U_I130_provenance.
- befree-20140225 importedOn "2014-02-25" NP785920.RAck5XKxXTiJpOjq-afEe1rkdz8MlN6WrOReybpqW7U_I130_provenance.