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- NP930205.RA3_92JTEu6RmO9PJGmxGukSqHHpglBQ3bJoUNyJzhQv0130_assertion type Assertion NP930205.RA3_92JTEu6RmO9PJGmxGukSqHHpglBQ3bJoUNyJzhQv0130_head.
- NP930205.RA3_92JTEu6RmO9PJGmxGukSqHHpglBQ3bJoUNyJzhQv0130_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." NP930205.RA3_92JTEu6RmO9PJGmxGukSqHHpglBQ3bJoUNyJzhQv0130_provenance.
- NP930205.RA3_92JTEu6RmO9PJGmxGukSqHHpglBQ3bJoUNyJzhQv0130_assertion evidence source_evidence_literature NP930205.RA3_92JTEu6RmO9PJGmxGukSqHHpglBQ3bJoUNyJzhQv0130_provenance.
- NP930205.RA3_92JTEu6RmO9PJGmxGukSqHHpglBQ3bJoUNyJzhQv0130_assertion SIO_000772 21989719 NP930205.RA3_92JTEu6RmO9PJGmxGukSqHHpglBQ3bJoUNyJzhQv0130_provenance.
- NP930205.RA3_92JTEu6RmO9PJGmxGukSqHHpglBQ3bJoUNyJzhQv0130_assertion wasDerivedFrom befree-2016 NP930205.RA3_92JTEu6RmO9PJGmxGukSqHHpglBQ3bJoUNyJzhQv0130_provenance.
- NP930205.RA3_92JTEu6RmO9PJGmxGukSqHHpglBQ3bJoUNyJzhQv0130_assertion wasGeneratedBy ECO_0000203 NP930205.RA3_92JTEu6RmO9PJGmxGukSqHHpglBQ3bJoUNyJzhQv0130_provenance.