Matches in Nanopublications for { <http://rdf.disgenet.org/nanopublications.trig#NP172299.RAgXlTYgaegOX8k8Wu8gMLQpAh6syla6bjre6dqkdKubc130_assertion> ?p ?o ?g. }
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- NP172299.RAgXlTYgaegOX8k8Wu8gMLQpAh6syla6bjre6dqkdKubc130_assertion type Assertion NP172299.RAgXlTYgaegOX8k8Wu8gMLQpAh6syla6bjre6dqkdKubc130_head.
- NP172299.RAgXlTYgaegOX8k8Wu8gMLQpAh6syla6bjre6dqkdKubc130_assertion description "[These results indicate a significant modification of the phenotype of FH with defective LDLR allele by EPHX2-287Arg variation in our studied kindred.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP172299.RAgXlTYgaegOX8k8Wu8gMLQpAh6syla6bjre6dqkdKubc130_provenance.
- NP172299.RAgXlTYgaegOX8k8Wu8gMLQpAh6syla6bjre6dqkdKubc130_assertion evidence source_evidence_literature NP172299.RAgXlTYgaegOX8k8Wu8gMLQpAh6syla6bjre6dqkdKubc130_provenance.
- NP172299.RAgXlTYgaegOX8k8Wu8gMLQpAh6syla6bjre6dqkdKubc130_assertion SIO_000772 14673705 NP172299.RAgXlTYgaegOX8k8Wu8gMLQpAh6syla6bjre6dqkdKubc130_provenance.
- NP172299.RAgXlTYgaegOX8k8Wu8gMLQpAh6syla6bjre6dqkdKubc130_assertion wasDerivedFrom befree-20140225 NP172299.RAgXlTYgaegOX8k8Wu8gMLQpAh6syla6bjre6dqkdKubc130_provenance.
- NP172299.RAgXlTYgaegOX8k8Wu8gMLQpAh6syla6bjre6dqkdKubc130_assertion wasGeneratedBy ECO_0000203 NP172299.RAgXlTYgaegOX8k8Wu8gMLQpAh6syla6bjre6dqkdKubc130_provenance.