Matches in Nanopublications for { <http://rdf.disgenet.org/nanopublications.trig#NP583468.RAk_UHerlF-DVyLi2-RDYhR3DcvCDXL6JKKSivaXvAjvk130_assertion> ?p ?o ?g. }
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- NP583468.RAk_UHerlF-DVyLi2-RDYhR3DcvCDXL6JKKSivaXvAjvk130_assertion type Assertion NP583468.RAk_UHerlF-DVyLi2-RDYhR3DcvCDXL6JKKSivaXvAjvk130_head.
- NP583468.RAk_UHerlF-DVyLi2-RDYhR3DcvCDXL6JKKSivaXvAjvk130_assertion description "[The identification of a causative mutation in ADAMTSL4 may allow the exclusion of Marfan syndrome in these families and guide the clinical management, of particular relevance in young children affected by EL.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP583468.RAk_UHerlF-DVyLi2-RDYhR3DcvCDXL6JKKSivaXvAjvk130_provenance.
- NP583468.RAk_UHerlF-DVyLi2-RDYhR3DcvCDXL6JKKSivaXvAjvk130_assertion evidence source_evidence_literature NP583468.RAk_UHerlF-DVyLi2-RDYhR3DcvCDXL6JKKSivaXvAjvk130_provenance.
- NP583468.RAk_UHerlF-DVyLi2-RDYhR3DcvCDXL6JKKSivaXvAjvk130_assertion SIO_000772 20564469 NP583468.RAk_UHerlF-DVyLi2-RDYhR3DcvCDXL6JKKSivaXvAjvk130_provenance.
- NP583468.RAk_UHerlF-DVyLi2-RDYhR3DcvCDXL6JKKSivaXvAjvk130_assertion wasDerivedFrom befree-20140225 NP583468.RAk_UHerlF-DVyLi2-RDYhR3DcvCDXL6JKKSivaXvAjvk130_provenance.
- NP583468.RAk_UHerlF-DVyLi2-RDYhR3DcvCDXL6JKKSivaXvAjvk130_assertion wasGeneratedBy ECO_0000203 NP583468.RAk_UHerlF-DVyLi2-RDYhR3DcvCDXL6JKKSivaXvAjvk130_provenance.