Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP1338663.RAiVidS8IBKc7TxfzGl3GUH0slf0_nn-H2sRH8UDwdkbU130_assertion> ?p ?o ?g. }
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- NP1338663.RAiVidS8IBKc7TxfzGl3GUH0slf0_nn-H2sRH8UDwdkbU130_assertion type Assertion NP1338663.RAiVidS8IBKc7TxfzGl3GUH0slf0_nn-H2sRH8UDwdkbU130_head.
- NP1338663.RAiVidS8IBKc7TxfzGl3GUH0slf0_nn-H2sRH8UDwdkbU130_assertion wasGeneratedBy ECO_0000203 NP1338663.RAiVidS8IBKc7TxfzGl3GUH0slf0_nn-H2sRH8UDwdkbU130_provenance.
- NP1338663.RAiVidS8IBKc7TxfzGl3GUH0slf0_nn-H2sRH8UDwdkbU130_assertion wasDerivedFrom befree-2016 NP1338663.RAiVidS8IBKc7TxfzGl3GUH0slf0_nn-H2sRH8UDwdkbU130_provenance.
- NP1338663.RAiVidS8IBKc7TxfzGl3GUH0slf0_nn-H2sRH8UDwdkbU130_assertion SIO_000772 8318557 NP1338663.RAiVidS8IBKc7TxfzGl3GUH0slf0_nn-H2sRH8UDwdkbU130_provenance.
- NP1338663.RAiVidS8IBKc7TxfzGl3GUH0slf0_nn-H2sRH8UDwdkbU130_assertion evidence source_evidence_literature NP1338663.RAiVidS8IBKc7TxfzGl3GUH0slf0_nn-H2sRH8UDwdkbU130_provenance.
- NP1338663.RAiVidS8IBKc7TxfzGl3GUH0slf0_nn-H2sRH8UDwdkbU130_assertion description "[We have recreated and expressed two known natural mutations within the LCAT gene which were reported on both alleles in a single case of familial LCAT deficiency.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1338663.RAiVidS8IBKc7TxfzGl3GUH0slf0_nn-H2sRH8UDwdkbU130_provenance.