Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP851891.RADskPVq2WVqSvZwsJVtWXCknSGPZAMYGiylXa8-EOLLc130_assertion> ?p ?o ?g. }
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- NP851891.RADskPVq2WVqSvZwsJVtWXCknSGPZAMYGiylXa8-EOLLc130_assertion type Assertion NP851891.RADskPVq2WVqSvZwsJVtWXCknSGPZAMYGiylXa8-EOLLc130_head.
- NP851891.RADskPVq2WVqSvZwsJVtWXCknSGPZAMYGiylXa8-EOLLc130_assertion description "[To analyse the possible association of HH with the C677T mutation in the MTHFR gene in SVT.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP851891.RADskPVq2WVqSvZwsJVtWXCknSGPZAMYGiylXa8-EOLLc130_provenance.
- NP851891.RADskPVq2WVqSvZwsJVtWXCknSGPZAMYGiylXa8-EOLLc130_assertion evidence source_evidence_literature NP851891.RADskPVq2WVqSvZwsJVtWXCknSGPZAMYGiylXa8-EOLLc130_provenance.
- NP851891.RADskPVq2WVqSvZwsJVtWXCknSGPZAMYGiylXa8-EOLLc130_assertion SIO_000772 21070369 NP851891.RADskPVq2WVqSvZwsJVtWXCknSGPZAMYGiylXa8-EOLLc130_provenance.
- NP851891.RADskPVq2WVqSvZwsJVtWXCknSGPZAMYGiylXa8-EOLLc130_assertion wasDerivedFrom befree-2016 NP851891.RADskPVq2WVqSvZwsJVtWXCknSGPZAMYGiylXa8-EOLLc130_provenance.
- NP851891.RADskPVq2WVqSvZwsJVtWXCknSGPZAMYGiylXa8-EOLLc130_assertion wasGeneratedBy ECO_0000203 NP851891.RADskPVq2WVqSvZwsJVtWXCknSGPZAMYGiylXa8-EOLLc130_provenance.