Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP400227.RAHZcpuvLpv_zF0xYUHNCL376i62UvbM6SIaWo613p1Fk130_assertion> ?p ?o ?g. }
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- NP400227.RAHZcpuvLpv_zF0xYUHNCL376i62UvbM6SIaWo613p1Fk130_assertion type Assertion NP400227.RAHZcpuvLpv_zF0xYUHNCL376i62UvbM6SIaWo613p1Fk130_head.
- NP400227.RAHZcpuvLpv_zF0xYUHNCL376i62UvbM6SIaWo613p1Fk130_assertion wasGeneratedBy ECO_0000203 NP400227.RAHZcpuvLpv_zF0xYUHNCL376i62UvbM6SIaWo613p1Fk130_provenance.
- NP400227.RAHZcpuvLpv_zF0xYUHNCL376i62UvbM6SIaWo613p1Fk130_assertion wasDerivedFrom befree-2016 NP400227.RAHZcpuvLpv_zF0xYUHNCL376i62UvbM6SIaWo613p1Fk130_provenance.
- NP400227.RAHZcpuvLpv_zF0xYUHNCL376i62UvbM6SIaWo613p1Fk130_assertion SIO_000772 12838562 NP400227.RAHZcpuvLpv_zF0xYUHNCL376i62UvbM6SIaWo613p1Fk130_provenance.
- NP400227.RAHZcpuvLpv_zF0xYUHNCL376i62UvbM6SIaWo613p1Fk130_assertion evidence source_evidence_literature NP400227.RAHZcpuvLpv_zF0xYUHNCL376i62UvbM6SIaWo613p1Fk130_provenance.
- NP400227.RAHZcpuvLpv_zF0xYUHNCL376i62UvbM6SIaWo613p1Fk130_assertion description "[While it is possible that defects of RECQL4 mRNA processing might account for part of the clinical variability observed for this syndrome, only a thorough analysis at both genomic and RNA level may allow a genotype-phenotype correlation in RTS patients, restricting the search of a second RTS locus to the specific patients.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP400227.RAHZcpuvLpv_zF0xYUHNCL376i62UvbM6SIaWo613p1Fk130_provenance.