Matches in Nanopublications for { <http://rdf.disgenet.org/nanopublications.trig#NP766809.RAEiaHa6cjIKZilahp4aFVB13YdUlnkyZaFBQ_mXKtD3w130_assertion> ?p ?o ?g. }
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- NP766809.RAEiaHa6cjIKZilahp4aFVB13YdUlnkyZaFBQ_mXKtD3w130_assertion type Assertion NP766809.RAEiaHa6cjIKZilahp4aFVB13YdUlnkyZaFBQ_mXKtD3w130_head.
- NP766809.RAEiaHa6cjIKZilahp4aFVB13YdUlnkyZaFBQ_mXKtD3w130_assertion description "[We did not identify other loss of function mutations in ABCA3 among patients with E292V that would account for their RDS.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP766809.RAEiaHa6cjIKZilahp4aFVB13YdUlnkyZaFBQ_mXKtD3w130_provenance.
- NP766809.RAEiaHa6cjIKZilahp4aFVB13YdUlnkyZaFBQ_mXKtD3w130_assertion evidence source_evidence_literature NP766809.RAEiaHa6cjIKZilahp4aFVB13YdUlnkyZaFBQ_mXKtD3w130_provenance.
- NP766809.RAEiaHa6cjIKZilahp4aFVB13YdUlnkyZaFBQ_mXKtD3w130_assertion SIO_000772 18317237 NP766809.RAEiaHa6cjIKZilahp4aFVB13YdUlnkyZaFBQ_mXKtD3w130_provenance.
- NP766809.RAEiaHa6cjIKZilahp4aFVB13YdUlnkyZaFBQ_mXKtD3w130_assertion wasDerivedFrom befree-20140225 NP766809.RAEiaHa6cjIKZilahp4aFVB13YdUlnkyZaFBQ_mXKtD3w130_provenance.
- NP766809.RAEiaHa6cjIKZilahp4aFVB13YdUlnkyZaFBQ_mXKtD3w130_assertion wasGeneratedBy ECO_0000203 NP766809.RAEiaHa6cjIKZilahp4aFVB13YdUlnkyZaFBQ_mXKtD3w130_provenance.