Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP14098.RAV5YZWjftlUTe96TTnVeFecCBl-U4K-L8__SX3om9sF8130_assertion> ?p ?o ?g. }
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- NP14098.RAV5YZWjftlUTe96TTnVeFecCBl-U4K-L8__SX3om9sF8130_assertion type Assertion NP14098.RAV5YZWjftlUTe96TTnVeFecCBl-U4K-L8__SX3om9sF8130_head.
- NP14098.RAV5YZWjftlUTe96TTnVeFecCBl-U4K-L8__SX3om9sF8130_assertion description "[We identified mutations in EXOSC3 in an additional 8 of 12 families with PCH1.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP14098.RAV5YZWjftlUTe96TTnVeFecCBl-U4K-L8__SX3om9sF8130_provenance.
- NP14098.RAV5YZWjftlUTe96TTnVeFecCBl-U4K-L8__SX3om9sF8130_assertion evidence source_evidence_curated NP14098.RAV5YZWjftlUTe96TTnVeFecCBl-U4K-L8__SX3om9sF8130_provenance.
- NP14098.RAV5YZWjftlUTe96TTnVeFecCBl-U4K-L8__SX3om9sF8130_assertion SIO_000772 22544365 NP14098.RAV5YZWjftlUTe96TTnVeFecCBl-U4K-L8__SX3om9sF8130_provenance.
- NP14098.RAV5YZWjftlUTe96TTnVeFecCBl-U4K-L8__SX3om9sF8130_assertion wasDerivedFrom ctd_human-20150221 NP14098.RAV5YZWjftlUTe96TTnVeFecCBl-U4K-L8__SX3om9sF8130_provenance.
- NP14098.RAV5YZWjftlUTe96TTnVeFecCBl-U4K-L8__SX3om9sF8130_assertion wasGeneratedBy ECO_0000218 NP14098.RAV5YZWjftlUTe96TTnVeFecCBl-U4K-L8__SX3om9sF8130_provenance.