Matches in Nanopublications for { <http://rdf.disgenet.org/nanopublications.trig#NP4101.RAXgfuEo_6Bofm0SdWQCWQhujsOFeFFLInl8YyLkGN-iY130_assertion> ?p ?o ?g. }
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- NP4101.RAXgfuEo_6Bofm0SdWQCWQhujsOFeFFLInl8YyLkGN-iY130_assertion type Assertion NP4101.RAXgfuEo_6Bofm0SdWQCWQhujsOFeFFLInl8YyLkGN-iY130_head.
- NP4101.RAXgfuEo_6Bofm0SdWQCWQhujsOFeFFLInl8YyLkGN-iY130_assertion wasGeneratedBy ECO_0000218 NP4101.RAXgfuEo_6Bofm0SdWQCWQhujsOFeFFLInl8YyLkGN-iY130_provenance.
- NP4101.RAXgfuEo_6Bofm0SdWQCWQhujsOFeFFLInl8YyLkGN-iY130_assertion wasDerivedFrom uniprot-20130724 NP4101.RAXgfuEo_6Bofm0SdWQCWQhujsOFeFFLInl8YyLkGN-iY130_provenance.
- NP4101.RAXgfuEo_6Bofm0SdWQCWQhujsOFeFFLInl8YyLkGN-iY130_assertion SIO_000772 11733564 NP4101.RAXgfuEo_6Bofm0SdWQCWQhujsOFeFFLInl8YyLkGN-iY130_provenance.
- NP4101.RAXgfuEo_6Bofm0SdWQCWQhujsOFeFFLInl8YyLkGN-iY130_assertion evidence source_evidence_curated NP4101.RAXgfuEo_6Bofm0SdWQCWQhujsOFeFFLInl8YyLkGN-iY130_provenance.
- NP4101.RAXgfuEo_6Bofm0SdWQCWQhujsOFeFFLInl8YyLkGN-iY130_assertion description "[MPDU1 mutations underlie a novel human congenital disorder of glycosylation, designated type If.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP4101.RAXgfuEo_6Bofm0SdWQCWQhujsOFeFFLInl8YyLkGN-iY130_provenance.