Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP930207.RANQGsOALjik4a864S1P89c9rSXF4ZLzsrjQ2vMzk9fbM130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP930207.RANQGsOALjik4a864S1P89c9rSXF4ZLzsrjQ2vMzk9fbM130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP930207.RANQGsOALjik4a864S1P89c9rSXF4ZLzsrjQ2vMzk9fbM130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP930207.RANQGsOALjik4a864S1P89c9rSXF4ZLzsrjQ2vMzk9fbM130_provenance.
- NP930207.RANQGsOALjik4a864S1P89c9rSXF4ZLzsrjQ2vMzk9fbM130_assertion description "[Dominant FBN1 mutations cause IEL or syndromic ectopia lentis (Marfan syndrome and Weill-Marchesani syndrome).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP930207.RANQGsOALjik4a864S1P89c9rSXF4ZLzsrjQ2vMzk9fbM130_provenance.
- NP930207.RANQGsOALjik4a864S1P89c9rSXF4ZLzsrjQ2vMzk9fbM130_assertion evidence source_evidence_literature NP930207.RANQGsOALjik4a864S1P89c9rSXF4ZLzsrjQ2vMzk9fbM130_provenance.
- NP930207.RANQGsOALjik4a864S1P89c9rSXF4ZLzsrjQ2vMzk9fbM130_assertion SIO_000772 21989719 NP930207.RANQGsOALjik4a864S1P89c9rSXF4ZLzsrjQ2vMzk9fbM130_provenance.
- NP930207.RANQGsOALjik4a864S1P89c9rSXF4ZLzsrjQ2vMzk9fbM130_assertion wasDerivedFrom befree-2016 NP930207.RANQGsOALjik4a864S1P89c9rSXF4ZLzsrjQ2vMzk9fbM130_provenance.
- NP930207.RANQGsOALjik4a864S1P89c9rSXF4ZLzsrjQ2vMzk9fbM130_assertion wasGeneratedBy ECO_0000203 NP930207.RANQGsOALjik4a864S1P89c9rSXF4ZLzsrjQ2vMzk9fbM130_provenance.
- befree-2016 importedOn "2016-02-19" NP930207.RANQGsOALjik4a864S1P89c9rSXF4ZLzsrjQ2vMzk9fbM130_provenance.