Matches in Nanopublications for { <http://rdf.disgenet.org/nanopublications.trig#NP338639.RApNse1uYfaP5SWBmFr0XHplH__dCjttkS3_7bYNJLA5Q130_assertion> ?p ?o ?g. }
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- NP338639.RApNse1uYfaP5SWBmFr0XHplH__dCjttkS3_7bYNJLA5Q130_assertion type Assertion NP338639.RApNse1uYfaP5SWBmFr0XHplH__dCjttkS3_7bYNJLA5Q130_head.
- NP338639.RApNse1uYfaP5SWBmFr0XHplH__dCjttkS3_7bYNJLA5Q130_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." NP338639.RApNse1uYfaP5SWBmFr0XHplH__dCjttkS3_7bYNJLA5Q130_provenance.
- NP338639.RApNse1uYfaP5SWBmFr0XHplH__dCjttkS3_7bYNJLA5Q130_assertion evidence source_evidence_literature NP338639.RApNse1uYfaP5SWBmFr0XHplH__dCjttkS3_7bYNJLA5Q130_provenance.
- NP338639.RApNse1uYfaP5SWBmFr0XHplH__dCjttkS3_7bYNJLA5Q130_assertion SIO_000772 19322210 NP338639.RApNse1uYfaP5SWBmFr0XHplH__dCjttkS3_7bYNJLA5Q130_provenance.
- NP338639.RApNse1uYfaP5SWBmFr0XHplH__dCjttkS3_7bYNJLA5Q130_assertion wasDerivedFrom befree-20140225 NP338639.RApNse1uYfaP5SWBmFr0XHplH__dCjttkS3_7bYNJLA5Q130_provenance.
- NP338639.RApNse1uYfaP5SWBmFr0XHplH__dCjttkS3_7bYNJLA5Q130_assertion wasGeneratedBy ECO_0000203 NP338639.RApNse1uYfaP5SWBmFr0XHplH__dCjttkS3_7bYNJLA5Q130_provenance.