Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP977215.RACX0MqmC7yoO2UNE5x7M2gO_R482ehDNmnUFaYLLGtoA130_assertion> ?p ?o ?g. }
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- NP977215.RACX0MqmC7yoO2UNE5x7M2gO_R482ehDNmnUFaYLLGtoA130_assertion type Assertion NP977215.RACX0MqmC7yoO2UNE5x7M2gO_R482ehDNmnUFaYLLGtoA130_head.
- NP977215.RACX0MqmC7yoO2UNE5x7M2gO_R482ehDNmnUFaYLLGtoA130_assertion description "[The absence of the phenotype of hereditary stomatocytosis implies that protein 7.2b deficiency plays no direct role in the etiology of this disorder and casts doubt on the previously proposed role of this protein as a mediator of cation transport in RBC.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP977215.RACX0MqmC7yoO2UNE5x7M2gO_R482ehDNmnUFaYLLGtoA130_provenance.
- NP977215.RACX0MqmC7yoO2UNE5x7M2gO_R482ehDNmnUFaYLLGtoA130_assertion evidence source_evidence_literature NP977215.RACX0MqmC7yoO2UNE5x7M2gO_R482ehDNmnUFaYLLGtoA130_provenance.
- NP977215.RACX0MqmC7yoO2UNE5x7M2gO_R482ehDNmnUFaYLLGtoA130_assertion SIO_000772 10090952 NP977215.RACX0MqmC7yoO2UNE5x7M2gO_R482ehDNmnUFaYLLGtoA130_provenance.
- NP977215.RACX0MqmC7yoO2UNE5x7M2gO_R482ehDNmnUFaYLLGtoA130_assertion wasDerivedFrom befree-20150227 NP977215.RACX0MqmC7yoO2UNE5x7M2gO_R482ehDNmnUFaYLLGtoA130_provenance.
- NP977215.RACX0MqmC7yoO2UNE5x7M2gO_R482ehDNmnUFaYLLGtoA130_assertion wasGeneratedBy ECO_0000203 NP977215.RACX0MqmC7yoO2UNE5x7M2gO_R482ehDNmnUFaYLLGtoA130_provenance.