Matches in Nanopublications for { <http://rdf.disgenet.org/nanopublications.trig#NP187877.RA_IMWTficPmlV-zhGPO4iCUoYVPnRFPrg3G1Wjtzn41c130_assertion> ?p ?o ?g. }
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- NP187877.RA_IMWTficPmlV-zhGPO4iCUoYVPnRFPrg3G1Wjtzn41c130_assertion type Assertion NP187877.RA_IMWTficPmlV-zhGPO4iCUoYVPnRFPrg3G1Wjtzn41c130_head.
- NP187877.RA_IMWTficPmlV-zhGPO4iCUoYVPnRFPrg3G1Wjtzn41c130_assertion wasGeneratedBy ECO_0000203 NP187877.RA_IMWTficPmlV-zhGPO4iCUoYVPnRFPrg3G1Wjtzn41c130_provenance.
- NP187877.RA_IMWTficPmlV-zhGPO4iCUoYVPnRFPrg3G1Wjtzn41c130_assertion wasDerivedFrom befree-20140225 NP187877.RA_IMWTficPmlV-zhGPO4iCUoYVPnRFPrg3G1Wjtzn41c130_provenance.
- NP187877.RA_IMWTficPmlV-zhGPO4iCUoYVPnRFPrg3G1Wjtzn41c130_assertion SIO_000772 14681881 NP187877.RA_IMWTficPmlV-zhGPO4iCUoYVPnRFPrg3G1Wjtzn41c130_provenance.
- NP187877.RA_IMWTficPmlV-zhGPO4iCUoYVPnRFPrg3G1Wjtzn41c130_assertion evidence source_evidence_literature NP187877.RA_IMWTficPmlV-zhGPO4iCUoYVPnRFPrg3G1Wjtzn41c130_provenance.
- NP187877.RA_IMWTficPmlV-zhGPO4iCUoYVPnRFPrg3G1Wjtzn41c130_assertion description "[Autosomal recessive spinal muscular atrophy with respiratory distress type 1 (SMARD1) is the second anterior horn cell disease in infants in which the genetic defect has been defined.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP187877.RA_IMWTficPmlV-zhGPO4iCUoYVPnRFPrg3G1Wjtzn41c130_provenance.