Matches in Nanopublications for { <http://rdf.disgenet.org/nanopublications.trig#NP59834.RAjIbFgX4xRKRtnk4KxWYPgXvoovGDA7AUkuR48L2oZKw130_assertion> ?p ?o ?g. }
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- NP59834.RAjIbFgX4xRKRtnk4KxWYPgXvoovGDA7AUkuR48L2oZKw130_assertion type Assertion NP59834.RAjIbFgX4xRKRtnk4KxWYPgXvoovGDA7AUkuR48L2oZKw130_head.
- NP59834.RAjIbFgX4xRKRtnk4KxWYPgXvoovGDA7AUkuR48L2oZKw130_assertion description "[It seems that examination of sporadic or familial MM cases for the 1100delC germline mutation in CHK2 is not justified. To evaluate whether this CHK2 founder mutation is associated with MM in patients with LFS syndrome, more MM cases from LFS families should be examined.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP59834.RAjIbFgX4xRKRtnk4KxWYPgXvoovGDA7AUkuR48L2oZKw130_provenance.
- NP59834.RAjIbFgX4xRKRtnk4KxWYPgXvoovGDA7AUkuR48L2oZKw130_assertion evidence source_evidence_literature NP59834.RAjIbFgX4xRKRtnk4KxWYPgXvoovGDA7AUkuR48L2oZKw130_provenance.
- NP59834.RAjIbFgX4xRKRtnk4KxWYPgXvoovGDA7AUkuR48L2oZKw130_assertion SIO_000772 15057041 NP59834.RAjIbFgX4xRKRtnk4KxWYPgXvoovGDA7AUkuR48L2oZKw130_provenance.
- NP59834.RAjIbFgX4xRKRtnk4KxWYPgXvoovGDA7AUkuR48L2oZKw130_assertion wasDerivedFrom gad-20130706 NP59834.RAjIbFgX4xRKRtnk4KxWYPgXvoovGDA7AUkuR48L2oZKw130_provenance.
- NP59834.RAjIbFgX4xRKRtnk4KxWYPgXvoovGDA7AUkuR48L2oZKw130_assertion wasGeneratedBy ECO_0000203 NP59834.RAjIbFgX4xRKRtnk4KxWYPgXvoovGDA7AUkuR48L2oZKw130_provenance.