Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP21874.RADxFMWAvYBRRP3CjI6gWvEKXRU0W_EfLFqInoPu2MpjA130_assertion> ?p ?o ?g. }
Showing items 1 to 6 of
6
with 100 items per page.
- NP21874.RADxFMWAvYBRRP3CjI6gWvEKXRU0W_EfLFqInoPu2MpjA130_assertion type Assertion NP21874.RADxFMWAvYBRRP3CjI6gWvEKXRU0W_EfLFqInoPu2MpjA130_head.
- NP21874.RADxFMWAvYBRRP3CjI6gWvEKXRU0W_EfLFqInoPu2MpjA130_assertion wasGeneratedBy ECO_0000218 NP21874.RADxFMWAvYBRRP3CjI6gWvEKXRU0W_EfLFqInoPu2MpjA130_provenance.
- NP21874.RADxFMWAvYBRRP3CjI6gWvEKXRU0W_EfLFqInoPu2MpjA130_assertion wasDerivedFrom ctd_human-2016 NP21874.RADxFMWAvYBRRP3CjI6gWvEKXRU0W_EfLFqInoPu2MpjA130_provenance.
- NP21874.RADxFMWAvYBRRP3CjI6gWvEKXRU0W_EfLFqInoPu2MpjA130_assertion SIO_000772 18519639 NP21874.RADxFMWAvYBRRP3CjI6gWvEKXRU0W_EfLFqInoPu2MpjA130_provenance.
- NP21874.RADxFMWAvYBRRP3CjI6gWvEKXRU0W_EfLFqInoPu2MpjA130_assertion evidence source_evidence_curated NP21874.RADxFMWAvYBRRP3CjI6gWvEKXRU0W_EfLFqInoPu2MpjA130_provenance.
- NP21874.RADxFMWAvYBRRP3CjI6gWvEKXRU0W_EfLFqInoPu2MpjA130_assertion description "[VACTERL/caudal regression/Currarino syndrome-like malformations in mice with mutation in the proprotein convertase Pcsk5.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP21874.RADxFMWAvYBRRP3CjI6gWvEKXRU0W_EfLFqInoPu2MpjA130_provenance.