Matches in Nanopublications for { <http://rdf.disgenet.org/nanopublications.trig#NP442683.RAF6X3JV3Q0CUs3G_Qc4UdwnzVcaLvA9L6ePsTx7mybkA130_assertion> ?p ?o ?g. }
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- NP442683.RAF6X3JV3Q0CUs3G_Qc4UdwnzVcaLvA9L6ePsTx7mybkA130_assertion type Assertion NP442683.RAF6X3JV3Q0CUs3G_Qc4UdwnzVcaLvA9L6ePsTx7mybkA130_head.
- NP442683.RAF6X3JV3Q0CUs3G_Qc4UdwnzVcaLvA9L6ePsTx7mybkA130_assertion description "[A systematic RNA interference screen to interrogate the function of each gene in the common deleted region (CDR) for the 5q- syndrome identified RPS14 as a critical haploinsufficiency disease gene for the erythroid failure, which is a characteristic of this syndrome.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP442683.RAF6X3JV3Q0CUs3G_Qc4UdwnzVcaLvA9L6ePsTx7mybkA130_provenance.
- NP442683.RAF6X3JV3Q0CUs3G_Qc4UdwnzVcaLvA9L6ePsTx7mybkA130_assertion evidence source_evidence_literature NP442683.RAF6X3JV3Q0CUs3G_Qc4UdwnzVcaLvA9L6ePsTx7mybkA130_provenance.
- NP442683.RAF6X3JV3Q0CUs3G_Qc4UdwnzVcaLvA9L6ePsTx7mybkA130_assertion SIO_000772 19322210 NP442683.RAF6X3JV3Q0CUs3G_Qc4UdwnzVcaLvA9L6ePsTx7mybkA130_provenance.
- NP442683.RAF6X3JV3Q0CUs3G_Qc4UdwnzVcaLvA9L6ePsTx7mybkA130_assertion wasDerivedFrom befree-20140225 NP442683.RAF6X3JV3Q0CUs3G_Qc4UdwnzVcaLvA9L6ePsTx7mybkA130_provenance.
- NP442683.RAF6X3JV3Q0CUs3G_Qc4UdwnzVcaLvA9L6ePsTx7mybkA130_assertion wasGeneratedBy ECO_0000203 NP442683.RAF6X3JV3Q0CUs3G_Qc4UdwnzVcaLvA9L6ePsTx7mybkA130_provenance.