Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP1247723.RAkCOlH4YVF0PY9E6PWueFIFk8nO4UKE1TjSmD2SBKk2o130_assertion> ?p ?o ?g. }
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- NP1247723.RAkCOlH4YVF0PY9E6PWueFIFk8nO4UKE1TjSmD2SBKk2o130_assertion description "[Identification of rare causal variants in sequence-based studies: methods and applications to VPS13B, a gene involved in Cohen syndrome and autism.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1247723.RAkCOlH4YVF0PY9E6PWueFIFk8nO4UKE1TjSmD2SBKk2o130_provenance.
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