Matches in Nanopublications for { <http://rdf.disgenet.org/nanopublications.trig#NP782878.RAwReeUMbZQWJAMO96UP1J_dwzgeJvkIKF9I8O1i2reL8130_assertion> ?p ?o ?g. }
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- NP782878.RAwReeUMbZQWJAMO96UP1J_dwzgeJvkIKF9I8O1i2reL8130_assertion type Assertion NP782878.RAwReeUMbZQWJAMO96UP1J_dwzgeJvkIKF9I8O1i2reL8130_head.
- NP782878.RAwReeUMbZQWJAMO96UP1J_dwzgeJvkIKF9I8O1i2reL8130_assertion description "[The present multiparameter analysis demonstrates the presumable direct involvement of the SP-B intron 4 deletion variant allele as a genetic risk factor to BPD.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP782878.RAwReeUMbZQWJAMO96UP1J_dwzgeJvkIKF9I8O1i2reL8130_provenance.
- NP782878.RAwReeUMbZQWJAMO96UP1J_dwzgeJvkIKF9I8O1i2reL8130_assertion evidence source_evidence_literature NP782878.RAwReeUMbZQWJAMO96UP1J_dwzgeJvkIKF9I8O1i2reL8130_provenance.
- NP782878.RAwReeUMbZQWJAMO96UP1J_dwzgeJvkIKF9I8O1i2reL8130_assertion SIO_000772 15102713 NP782878.RAwReeUMbZQWJAMO96UP1J_dwzgeJvkIKF9I8O1i2reL8130_provenance.
- NP782878.RAwReeUMbZQWJAMO96UP1J_dwzgeJvkIKF9I8O1i2reL8130_assertion wasDerivedFrom befree-20140225 NP782878.RAwReeUMbZQWJAMO96UP1J_dwzgeJvkIKF9I8O1i2reL8130_provenance.
- NP782878.RAwReeUMbZQWJAMO96UP1J_dwzgeJvkIKF9I8O1i2reL8130_assertion wasGeneratedBy ECO_0000203 NP782878.RAwReeUMbZQWJAMO96UP1J_dwzgeJvkIKF9I8O1i2reL8130_provenance.