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- source_evidence_literature type ECO_0000212 NP922532.RA-x6HbWMWHavsg1yWa4QCv5DA6fXoeCrfBKSN7Ro_upk130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP922532.RA-x6HbWMWHavsg1yWa4QCv5DA6fXoeCrfBKSN7Ro_upk130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP922532.RA-x6HbWMWHavsg1yWa4QCv5DA6fXoeCrfBKSN7Ro_upk130_provenance.
- 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.
- befree-20140225 importedOn "2014-02-25" NP922532.RA-x6HbWMWHavsg1yWa4QCv5DA6fXoeCrfBKSN7Ro_upk130_provenance.