Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP801796.RAO4g5vL0oJPisSI3htFL2zLrQcqoYw009zZCMVbdaAU0130_assertion> ?p ?o ?g. }
Showing items 1 to 6 of
6
with 100 items per page.
- NP801796.RAO4g5vL0oJPisSI3htFL2zLrQcqoYw009zZCMVbdaAU0130_assertion type Assertion NP801796.RAO4g5vL0oJPisSI3htFL2zLrQcqoYw009zZCMVbdaAU0130_head.
- NP801796.RAO4g5vL0oJPisSI3htFL2zLrQcqoYw009zZCMVbdaAU0130_assertion description "[These results suggest that STX11 gene mutations may be associated with secondary malignancies (MDS/AML), and that there is segregation of specific clinical features in FHL patients with an underlying genotype.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP801796.RAO4g5vL0oJPisSI3htFL2zLrQcqoYw009zZCMVbdaAU0130_provenance.
- NP801796.RAO4g5vL0oJPisSI3htFL2zLrQcqoYw009zZCMVbdaAU0130_assertion evidence source_evidence_literature NP801796.RAO4g5vL0oJPisSI3htFL2zLrQcqoYw009zZCMVbdaAU0130_provenance.
- NP801796.RAO4g5vL0oJPisSI3htFL2zLrQcqoYw009zZCMVbdaAU0130_assertion SIO_000772 16582076 NP801796.RAO4g5vL0oJPisSI3htFL2zLrQcqoYw009zZCMVbdaAU0130_provenance.
- NP801796.RAO4g5vL0oJPisSI3htFL2zLrQcqoYw009zZCMVbdaAU0130_assertion wasDerivedFrom befree-20150227 NP801796.RAO4g5vL0oJPisSI3htFL2zLrQcqoYw009zZCMVbdaAU0130_provenance.
- NP801796.RAO4g5vL0oJPisSI3htFL2zLrQcqoYw009zZCMVbdaAU0130_assertion wasGeneratedBy ECO_0000203 NP801796.RAO4g5vL0oJPisSI3htFL2zLrQcqoYw009zZCMVbdaAU0130_provenance.