Matches in Nanopublications for { <http://rdf.disgenet.org/nanopublications.trig#NP599206.RAYKFpfyb73TUGGvCmCUaRLNwUeT_PB2PzFeIvW8cM7JE130_assertion> ?p ?o ?g. }
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- NP599206.RAYKFpfyb73TUGGvCmCUaRLNwUeT_PB2PzFeIvW8cM7JE130_assertion type Assertion NP599206.RAYKFpfyb73TUGGvCmCUaRLNwUeT_PB2PzFeIvW8cM7JE130_head.
- NP599206.RAYKFpfyb73TUGGvCmCUaRLNwUeT_PB2PzFeIvW8cM7JE130_assertion description "[A multi-copy microsatellite marker that is deleted in more than 90% of type I SMA chromosomes is embedded in an intron of this gene, indicating that H4F5 is also highly deleted in type I SMA chromosomes, and thus is a candidate phenotypic modifier for SMA.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP599206.RAYKFpfyb73TUGGvCmCUaRLNwUeT_PB2PzFeIvW8cM7JE130_provenance.
- NP599206.RAYKFpfyb73TUGGvCmCUaRLNwUeT_PB2PzFeIvW8cM7JE130_assertion evidence source_evidence_literature NP599206.RAYKFpfyb73TUGGvCmCUaRLNwUeT_PB2PzFeIvW8cM7JE130_provenance.
- NP599206.RAYKFpfyb73TUGGvCmCUaRLNwUeT_PB2PzFeIvW8cM7JE130_assertion SIO_000772 9731538 NP599206.RAYKFpfyb73TUGGvCmCUaRLNwUeT_PB2PzFeIvW8cM7JE130_provenance.
- NP599206.RAYKFpfyb73TUGGvCmCUaRLNwUeT_PB2PzFeIvW8cM7JE130_assertion wasDerivedFrom befree-20140225 NP599206.RAYKFpfyb73TUGGvCmCUaRLNwUeT_PB2PzFeIvW8cM7JE130_provenance.
- NP599206.RAYKFpfyb73TUGGvCmCUaRLNwUeT_PB2PzFeIvW8cM7JE130_assertion wasGeneratedBy ECO_0000203 NP599206.RAYKFpfyb73TUGGvCmCUaRLNwUeT_PB2PzFeIvW8cM7JE130_provenance.