Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP1355855.RAtHYlChST0MlZle0cnrXTYuFZohE54Z_U14kly5-1QFc130_assertion> ?p ?o ?g. }
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- NP1355855.RAtHYlChST0MlZle0cnrXTYuFZohE54Z_U14kly5-1QFc130_assertion type Assertion NP1355855.RAtHYlChST0MlZle0cnrXTYuFZohE54Z_U14kly5-1QFc130_head.
- NP1355855.RAtHYlChST0MlZle0cnrXTYuFZohE54Z_U14kly5-1QFc130_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." NP1355855.RAtHYlChST0MlZle0cnrXTYuFZohE54Z_U14kly5-1QFc130_provenance.
- NP1355855.RAtHYlChST0MlZle0cnrXTYuFZohE54Z_U14kly5-1QFc130_assertion evidence source_evidence_literature NP1355855.RAtHYlChST0MlZle0cnrXTYuFZohE54Z_U14kly5-1QFc130_provenance.
- NP1355855.RAtHYlChST0MlZle0cnrXTYuFZohE54Z_U14kly5-1QFc130_assertion SIO_000772 8765219 NP1355855.RAtHYlChST0MlZle0cnrXTYuFZohE54Z_U14kly5-1QFc130_provenance.
- NP1355855.RAtHYlChST0MlZle0cnrXTYuFZohE54Z_U14kly5-1QFc130_assertion wasDerivedFrom befree-2016 NP1355855.RAtHYlChST0MlZle0cnrXTYuFZohE54Z_U14kly5-1QFc130_provenance.
- NP1355855.RAtHYlChST0MlZle0cnrXTYuFZohE54Z_U14kly5-1QFc130_assertion wasGeneratedBy ECO_0000203 NP1355855.RAtHYlChST0MlZle0cnrXTYuFZohE54Z_U14kly5-1QFc130_provenance.