Matches in Nanopublications for { <http://rdf.disgenet.org/nanopublications.trig#NP293272.RAWUuiH0wOJ2Bn7Do9TdmGtwF2nqWmbaAgtH8o7TcLGgU130_assertion> ?p ?o ?g. }
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- NP293272.RAWUuiH0wOJ2Bn7Do9TdmGtwF2nqWmbaAgtH8o7TcLGgU130_assertion type Assertion NP293272.RAWUuiH0wOJ2Bn7Do9TdmGtwF2nqWmbaAgtH8o7TcLGgU130_head.
- NP293272.RAWUuiH0wOJ2Bn7Do9TdmGtwF2nqWmbaAgtH8o7TcLGgU130_assertion wasGeneratedBy ECO_0000203 NP293272.RAWUuiH0wOJ2Bn7Do9TdmGtwF2nqWmbaAgtH8o7TcLGgU130_provenance.
- NP293272.RAWUuiH0wOJ2Bn7Do9TdmGtwF2nqWmbaAgtH8o7TcLGgU130_assertion wasDerivedFrom befree-20140225 NP293272.RAWUuiH0wOJ2Bn7Do9TdmGtwF2nqWmbaAgtH8o7TcLGgU130_provenance.
- NP293272.RAWUuiH0wOJ2Bn7Do9TdmGtwF2nqWmbaAgtH8o7TcLGgU130_assertion SIO_000772 21236492 NP293272.RAWUuiH0wOJ2Bn7Do9TdmGtwF2nqWmbaAgtH8o7TcLGgU130_provenance.
- NP293272.RAWUuiH0wOJ2Bn7Do9TdmGtwF2nqWmbaAgtH8o7TcLGgU130_assertion evidence source_evidence_literature NP293272.RAWUuiH0wOJ2Bn7Do9TdmGtwF2nqWmbaAgtH8o7TcLGgU130_provenance.
- NP293272.RAWUuiH0wOJ2Bn7Do9TdmGtwF2nqWmbaAgtH8o7TcLGgU130_assertion description "[To describe a novel laminin β-2 (LAMB2) mutation associated with nephrotic syndrome and severe retinal disease without microcoria in a large, multigenerational family with Pierson syndrome.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP293272.RAWUuiH0wOJ2Bn7Do9TdmGtwF2nqWmbaAgtH8o7TcLGgU130_provenance.