Matches in Nanopublications for { <http://rdf.disgenet.org/nanopublications.trig#NP517996.RAk6EhAzkyQcW9EL7HNlAIJsTtP0tLAmwmV4cuwfAb7kA130_assertion> ?p ?o ?g. }
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- NP517996.RAk6EhAzkyQcW9EL7HNlAIJsTtP0tLAmwmV4cuwfAb7kA130_assertion type Assertion NP517996.RAk6EhAzkyQcW9EL7HNlAIJsTtP0tLAmwmV4cuwfAb7kA130_head.
- NP517996.RAk6EhAzkyQcW9EL7HNlAIJsTtP0tLAmwmV4cuwfAb7kA130_assertion description "[Here, in an individual, we demonstrate that a homozygous novel mutation in the MMR gene MSH2 is associated with leukemia and multiple caf�-au-lait spots, a feature of neurofibromatosis type 1.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP517996.RAk6EhAzkyQcW9EL7HNlAIJsTtP0tLAmwmV4cuwfAb7kA130_provenance.
- NP517996.RAk6EhAzkyQcW9EL7HNlAIJsTtP0tLAmwmV4cuwfAb7kA130_assertion evidence source_evidence_literature NP517996.RAk6EhAzkyQcW9EL7HNlAIJsTtP0tLAmwmV4cuwfAb7kA130_provenance.
- NP517996.RAk6EhAzkyQcW9EL7HNlAIJsTtP0tLAmwmV4cuwfAb7kA130_assertion SIO_000772 11809679 NP517996.RAk6EhAzkyQcW9EL7HNlAIJsTtP0tLAmwmV4cuwfAb7kA130_provenance.
- NP517996.RAk6EhAzkyQcW9EL7HNlAIJsTtP0tLAmwmV4cuwfAb7kA130_assertion wasDerivedFrom befree-20140225 NP517996.RAk6EhAzkyQcW9EL7HNlAIJsTtP0tLAmwmV4cuwfAb7kA130_provenance.
- NP517996.RAk6EhAzkyQcW9EL7HNlAIJsTtP0tLAmwmV4cuwfAb7kA130_assertion wasGeneratedBy ECO_0000203 NP517996.RAk6EhAzkyQcW9EL7HNlAIJsTtP0tLAmwmV4cuwfAb7kA130_provenance.