Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP356199.RAAM9SM1RNB2Y28vNFS93y8vwNbQ7iCHhFCR5hwnYUXX0130_assertion> ?p ?o ?g. }
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- NP356199.RAAM9SM1RNB2Y28vNFS93y8vwNbQ7iCHhFCR5hwnYUXX0130_assertion type Assertion NP356199.RAAM9SM1RNB2Y28vNFS93y8vwNbQ7iCHhFCR5hwnYUXX0130_head.
- NP356199.RAAM9SM1RNB2Y28vNFS93y8vwNbQ7iCHhFCR5hwnYUXX0130_assertion description "[Using expression microarrays and a unique method for comparative expression analysis called L2L, we sought to define this defect in cells lacking a functional CS group B (CSB) protein, the SWI/SNF-like ATPase responsible for most cases of CS.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP356199.RAAM9SM1RNB2Y28vNFS93y8vwNbQ7iCHhFCR5hwnYUXX0130_provenance.
- NP356199.RAAM9SM1RNB2Y28vNFS93y8vwNbQ7iCHhFCR5hwnYUXX0130_assertion evidence source_evidence_literature NP356199.RAAM9SM1RNB2Y28vNFS93y8vwNbQ7iCHhFCR5hwnYUXX0130_provenance.
- NP356199.RAAM9SM1RNB2Y28vNFS93y8vwNbQ7iCHhFCR5hwnYUXX0130_assertion SIO_000772 16772382 NP356199.RAAM9SM1RNB2Y28vNFS93y8vwNbQ7iCHhFCR5hwnYUXX0130_provenance.
- NP356199.RAAM9SM1RNB2Y28vNFS93y8vwNbQ7iCHhFCR5hwnYUXX0130_assertion wasDerivedFrom befree-20150227 NP356199.RAAM9SM1RNB2Y28vNFS93y8vwNbQ7iCHhFCR5hwnYUXX0130_provenance.
- NP356199.RAAM9SM1RNB2Y28vNFS93y8vwNbQ7iCHhFCR5hwnYUXX0130_assertion wasGeneratedBy ECO_0000203 NP356199.RAAM9SM1RNB2Y28vNFS93y8vwNbQ7iCHhFCR5hwnYUXX0130_provenance.