Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP9107.RA3Khck3CeK2v7YXS9VsjPVRPWbLkIHAHlJz3kKH_TvW8130_assertion> ?p ?o ?g. }
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- NP9107.RA3Khck3CeK2v7YXS9VsjPVRPWbLkIHAHlJz3kKH_TvW8130_assertion type Assertion NP9107.RA3Khck3CeK2v7YXS9VsjPVRPWbLkIHAHlJz3kKH_TvW8130_head.
- NP9107.RA3Khck3CeK2v7YXS9VsjPVRPWbLkIHAHlJz3kKH_TvW8130_assertion description "[Molecular basis for protein S hereditary deficiency: genetic defects observed in 118 patients with type I and type IIa deficiencies. The French Network on Molecular Abnormalities Responsible for Protein C and Protein S Deficiencies.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP9107.RA3Khck3CeK2v7YXS9VsjPVRPWbLkIHAHlJz3kKH_TvW8130_provenance.
- NP9107.RA3Khck3CeK2v7YXS9VsjPVRPWbLkIHAHlJz3kKH_TvW8130_assertion evidence source_evidence_curated NP9107.RA3Khck3CeK2v7YXS9VsjPVRPWbLkIHAHlJz3kKH_TvW8130_provenance.
- NP9107.RA3Khck3CeK2v7YXS9VsjPVRPWbLkIHAHlJz3kKH_TvW8130_assertion SIO_000772 8765219 NP9107.RA3Khck3CeK2v7YXS9VsjPVRPWbLkIHAHlJz3kKH_TvW8130_provenance.
- NP9107.RA3Khck3CeK2v7YXS9VsjPVRPWbLkIHAHlJz3kKH_TvW8130_assertion wasDerivedFrom uniprot-2016 NP9107.RA3Khck3CeK2v7YXS9VsjPVRPWbLkIHAHlJz3kKH_TvW8130_provenance.
- NP9107.RA3Khck3CeK2v7YXS9VsjPVRPWbLkIHAHlJz3kKH_TvW8130_assertion wasGeneratedBy ECO_0000218 NP9107.RA3Khck3CeK2v7YXS9VsjPVRPWbLkIHAHlJz3kKH_TvW8130_provenance.