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- NP742033.RAMWujB1LbYSCkI43psVPbguL34o76zgbpb-En4yhq4Q0130_assertion type Assertion NP742033.RAMWujB1LbYSCkI43psVPbguL34o76zgbpb-En4yhq4Q0130_head.
- NP742033.RAMWujB1LbYSCkI43psVPbguL34o76zgbpb-En4yhq4Q0130_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." NP742033.RAMWujB1LbYSCkI43psVPbguL34o76zgbpb-En4yhq4Q0130_provenance.
- NP742033.RAMWujB1LbYSCkI43psVPbguL34o76zgbpb-En4yhq4Q0130_assertion evidence source_evidence_literature NP742033.RAMWujB1LbYSCkI43psVPbguL34o76zgbpb-En4yhq4Q0130_provenance.
- NP742033.RAMWujB1LbYSCkI43psVPbguL34o76zgbpb-En4yhq4Q0130_assertion SIO_000772 21989719 NP742033.RAMWujB1LbYSCkI43psVPbguL34o76zgbpb-En4yhq4Q0130_provenance.
- NP742033.RAMWujB1LbYSCkI43psVPbguL34o76zgbpb-En4yhq4Q0130_assertion wasDerivedFrom befree-20140225 NP742033.RAMWujB1LbYSCkI43psVPbguL34o76zgbpb-En4yhq4Q0130_provenance.
- NP742033.RAMWujB1LbYSCkI43psVPbguL34o76zgbpb-En4yhq4Q0130_assertion wasGeneratedBy ECO_0000203 NP742033.RAMWujB1LbYSCkI43psVPbguL34o76zgbpb-En4yhq4Q0130_provenance.