Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP828386.RAW6VDsXD4NzdhW_hIZ_wIa8j-JJr6cFFaiehu0k_TbLo130_assertion> ?p ?o ?g. }
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- NP828386.RAW6VDsXD4NzdhW_hIZ_wIa8j-JJr6cFFaiehu0k_TbLo130_assertion type Assertion NP828386.RAW6VDsXD4NzdhW_hIZ_wIa8j-JJr6cFFaiehu0k_TbLo130_head.
- NP828386.RAW6VDsXD4NzdhW_hIZ_wIa8j-JJr6cFFaiehu0k_TbLo130_assertion wasGeneratedBy ECO_0000203 NP828386.RAW6VDsXD4NzdhW_hIZ_wIa8j-JJr6cFFaiehu0k_TbLo130_provenance.
- NP828386.RAW6VDsXD4NzdhW_hIZ_wIa8j-JJr6cFFaiehu0k_TbLo130_assertion wasDerivedFrom befree-2016 NP828386.RAW6VDsXD4NzdhW_hIZ_wIa8j-JJr6cFFaiehu0k_TbLo130_provenance.
- NP828386.RAW6VDsXD4NzdhW_hIZ_wIa8j-JJr6cFFaiehu0k_TbLo130_assertion SIO_000772 20660572 NP828386.RAW6VDsXD4NzdhW_hIZ_wIa8j-JJr6cFFaiehu0k_TbLo130_provenance.
- NP828386.RAW6VDsXD4NzdhW_hIZ_wIa8j-JJr6cFFaiehu0k_TbLo130_assertion evidence source_evidence_literature NP828386.RAW6VDsXD4NzdhW_hIZ_wIa8j-JJr6cFFaiehu0k_TbLo130_provenance.
- NP828386.RAW6VDsXD4NzdhW_hIZ_wIa8j-JJr6cFFaiehu0k_TbLo130_assertion description "[In the NET-Registry, 9/101 patients (8.9%) with ICTs had germline mutations, 8 in MEN1 and 1 in VHL.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP828386.RAW6VDsXD4NzdhW_hIZ_wIa8j-JJr6cFFaiehu0k_TbLo130_provenance.