Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP396004.RAEA_2nyZsXTtTJxNRK7z1Ct7GTatiQrkF14P2gBMHyCo130_assertion> ?p ?o ?g. }
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- NP396004.RAEA_2nyZsXTtTJxNRK7z1Ct7GTatiQrkF14P2gBMHyCo130_assertion type Assertion NP396004.RAEA_2nyZsXTtTJxNRK7z1Ct7GTatiQrkF14P2gBMHyCo130_head.
- NP396004.RAEA_2nyZsXTtTJxNRK7z1Ct7GTatiQrkF14P2gBMHyCo130_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." NP396004.RAEA_2nyZsXTtTJxNRK7z1Ct7GTatiQrkF14P2gBMHyCo130_provenance.
- NP396004.RAEA_2nyZsXTtTJxNRK7z1Ct7GTatiQrkF14P2gBMHyCo130_assertion evidence source_evidence_literature NP396004.RAEA_2nyZsXTtTJxNRK7z1Ct7GTatiQrkF14P2gBMHyCo130_provenance.
- NP396004.RAEA_2nyZsXTtTJxNRK7z1Ct7GTatiQrkF14P2gBMHyCo130_assertion SIO_000772 21989719 NP396004.RAEA_2nyZsXTtTJxNRK7z1Ct7GTatiQrkF14P2gBMHyCo130_provenance.
- NP396004.RAEA_2nyZsXTtTJxNRK7z1Ct7GTatiQrkF14P2gBMHyCo130_assertion wasDerivedFrom befree-20150227 NP396004.RAEA_2nyZsXTtTJxNRK7z1Ct7GTatiQrkF14P2gBMHyCo130_provenance.
- NP396004.RAEA_2nyZsXTtTJxNRK7z1Ct7GTatiQrkF14P2gBMHyCo130_assertion wasGeneratedBy ECO_0000203 NP396004.RAEA_2nyZsXTtTJxNRK7z1Ct7GTatiQrkF14P2gBMHyCo130_provenance.