Matches in Nanopublications for { <http://rdf.disgenet.org/nanopublications.trig#NP922532.RA-x6HbWMWHavsg1yWa4QCv5DA6fXoeCrfBKSN7Ro_upk130_assertion> ?p ?o ?g. }
Showing items 1 to 6 of
6
with 100 items per page.
- NP922532.RA-x6HbWMWHavsg1yWa4QCv5DA6fXoeCrfBKSN7Ro_upk130_assertion type Assertion NP922532.RA-x6HbWMWHavsg1yWa4QCv5DA6fXoeCrfBKSN7Ro_upk130_head.
- NP922532.RA-x6HbWMWHavsg1yWa4QCv5DA6fXoeCrfBKSN7Ro_upk130_assertion description "[Mutations in FLCN are also responsible for Birt-Hogg-Dub� (BHD) syndrome (a dominantly inherited disease characterized by benign skin tumors, PSP, and diverse types of renal cancer) and, rarely, are detected in sporadic renal and colorectal tumors.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP922532.RA-x6HbWMWHavsg1yWa4QCv5DA6fXoeCrfBKSN7Ro_upk130_provenance.
- NP922532.RA-x6HbWMWHavsg1yWa4QCv5DA6fXoeCrfBKSN7Ro_upk130_assertion evidence source_evidence_literature NP922532.RA-x6HbWMWHavsg1yWa4QCv5DA6fXoeCrfBKSN7Ro_upk130_provenance.
- NP922532.RA-x6HbWMWHavsg1yWa4QCv5DA6fXoeCrfBKSN7Ro_upk130_assertion SIO_000772 15657874 NP922532.RA-x6HbWMWHavsg1yWa4QCv5DA6fXoeCrfBKSN7Ro_upk130_provenance.
- NP922532.RA-x6HbWMWHavsg1yWa4QCv5DA6fXoeCrfBKSN7Ro_upk130_assertion wasDerivedFrom befree-20140225 NP922532.RA-x6HbWMWHavsg1yWa4QCv5DA6fXoeCrfBKSN7Ro_upk130_provenance.
- NP922532.RA-x6HbWMWHavsg1yWa4QCv5DA6fXoeCrfBKSN7Ro_upk130_assertion wasGeneratedBy ECO_0000203 NP922532.RA-x6HbWMWHavsg1yWa4QCv5DA6fXoeCrfBKSN7Ro_upk130_provenance.