Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP339435.RACeVUnEWg8mEoFp1KTkCBjFtW6P2frRT-3S_lc1ACG8Q130_assertion> ?p ?o ?g. }
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- NP339435.RACeVUnEWg8mEoFp1KTkCBjFtW6P2frRT-3S_lc1ACG8Q130_assertion type Assertion NP339435.RACeVUnEWg8mEoFp1KTkCBjFtW6P2frRT-3S_lc1ACG8Q130_head.
- NP339435.RACeVUnEWg8mEoFp1KTkCBjFtW6P2frRT-3S_lc1ACG8Q130_assertion wasGeneratedBy ECO_0000203 NP339435.RACeVUnEWg8mEoFp1KTkCBjFtW6P2frRT-3S_lc1ACG8Q130_provenance.
- NP339435.RACeVUnEWg8mEoFp1KTkCBjFtW6P2frRT-3S_lc1ACG8Q130_assertion wasDerivedFrom befree-2016 NP339435.RACeVUnEWg8mEoFp1KTkCBjFtW6P2frRT-3S_lc1ACG8Q130_provenance.
- NP339435.RACeVUnEWg8mEoFp1KTkCBjFtW6P2frRT-3S_lc1ACG8Q130_assertion SIO_000772 11749051 NP339435.RACeVUnEWg8mEoFp1KTkCBjFtW6P2frRT-3S_lc1ACG8Q130_provenance.
- NP339435.RACeVUnEWg8mEoFp1KTkCBjFtW6P2frRT-3S_lc1ACG8Q130_assertion evidence source_evidence_literature NP339435.RACeVUnEWg8mEoFp1KTkCBjFtW6P2frRT-3S_lc1ACG8Q130_provenance.
- NP339435.RACeVUnEWg8mEoFp1KTkCBjFtW6P2frRT-3S_lc1ACG8Q130_assertion description "[Hence, autosomal dominant inclusion body myopathy (HIBM), Paget disease of bone (PDB), and frontotemporal dementia (FTD) localizes to a 1.08-6.46 cM critical interval on 9p13.3-12 in the region of autosomal recessive IBM2.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP339435.RACeVUnEWg8mEoFp1KTkCBjFtW6P2frRT-3S_lc1ACG8Q130_provenance.