Matches in Nanopublications for { <http://rdf.disgenet.org/nanopublications.trig#NP414953.RAU_DFDTQJA5OPAcW4yguKftUtF2fipQ82JgtUTs2GjCU130_assertion> ?p ?o ?g. }
Showing items 1 to 6 of
6
with 100 items per page.
- NP414953.RAU_DFDTQJA5OPAcW4yguKftUtF2fipQ82JgtUTs2GjCU130_assertion type Assertion NP414953.RAU_DFDTQJA5OPAcW4yguKftUtF2fipQ82JgtUTs2GjCU130_head.
- NP414953.RAU_DFDTQJA5OPAcW4yguKftUtF2fipQ82JgtUTs2GjCU130_assertion description "[In 166 patients (25.9%) the disease was familial and caused by germline mutations in VHL (56), SDHB (34), SDHD (31), RET (31) or NF1 (14), causing von Hippel-Lindau disease, SDHB- or SDHD-PH/FPGL syndromes, multiple endocrine neoplasia type 2 (MEN 2) and type 1 neurofibromatosis (NF1), respectively.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP414953.RAU_DFDTQJA5OPAcW4yguKftUtF2fipQ82JgtUTs2GjCU130_provenance.
- NP414953.RAU_DFDTQJA5OPAcW4yguKftUtF2fipQ82JgtUTs2GjCU130_assertion evidence source_evidence_literature NP414953.RAU_DFDTQJA5OPAcW4yguKftUtF2fipQ82JgtUTs2GjCU130_provenance.
- NP414953.RAU_DFDTQJA5OPAcW4yguKftUtF2fipQ82JgtUTs2GjCU130_assertion SIO_000772 17121518 NP414953.RAU_DFDTQJA5OPAcW4yguKftUtF2fipQ82JgtUTs2GjCU130_provenance.
- NP414953.RAU_DFDTQJA5OPAcW4yguKftUtF2fipQ82JgtUTs2GjCU130_assertion wasDerivedFrom befree-20140225 NP414953.RAU_DFDTQJA5OPAcW4yguKftUtF2fipQ82JgtUTs2GjCU130_provenance.
- NP414953.RAU_DFDTQJA5OPAcW4yguKftUtF2fipQ82JgtUTs2GjCU130_assertion wasGeneratedBy ECO_0000203 NP414953.RAU_DFDTQJA5OPAcW4yguKftUtF2fipQ82JgtUTs2GjCU130_provenance.