Matches in Nanopublications for { <http://rdf.disgenet.org/nanopublications.trig#NP474223.RAAF47Peye60HVHZOq2qfdXswdX0bht0cv1yD9WQtRrlU130_assertion> ?p ?o ?g. }
Showing items 1 to 6 of
6
with 100 items per page.
- NP474223.RAAF47Peye60HVHZOq2qfdXswdX0bht0cv1yD9WQtRrlU130_assertion type Assertion NP474223.RAAF47Peye60HVHZOq2qfdXswdX0bht0cv1yD9WQtRrlU130_head.
- NP474223.RAAF47Peye60HVHZOq2qfdXswdX0bht0cv1yD9WQtRrlU130_assertion description "[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." NP474223.RAAF47Peye60HVHZOq2qfdXswdX0bht0cv1yD9WQtRrlU130_provenance.
- NP474223.RAAF47Peye60HVHZOq2qfdXswdX0bht0cv1yD9WQtRrlU130_assertion evidence source_evidence_literature NP474223.RAAF47Peye60HVHZOq2qfdXswdX0bht0cv1yD9WQtRrlU130_provenance.
- NP474223.RAAF47Peye60HVHZOq2qfdXswdX0bht0cv1yD9WQtRrlU130_assertion SIO_000772 15057041 NP474223.RAAF47Peye60HVHZOq2qfdXswdX0bht0cv1yD9WQtRrlU130_provenance.
- NP474223.RAAF47Peye60HVHZOq2qfdXswdX0bht0cv1yD9WQtRrlU130_assertion wasDerivedFrom befree-20140225 NP474223.RAAF47Peye60HVHZOq2qfdXswdX0bht0cv1yD9WQtRrlU130_provenance.
- NP474223.RAAF47Peye60HVHZOq2qfdXswdX0bht0cv1yD9WQtRrlU130_assertion wasGeneratedBy ECO_0000203 NP474223.RAAF47Peye60HVHZOq2qfdXswdX0bht0cv1yD9WQtRrlU130_provenance.