Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP662828.RAe7FbvLlKIYiTp_aBfSBZjNOrPP9g_XTWEFOqYhVOL78130_assertion> ?p ?o ?g. }
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- NP662828.RAe7FbvLlKIYiTp_aBfSBZjNOrPP9g_XTWEFOqYhVOL78130_assertion type Assertion NP662828.RAe7FbvLlKIYiTp_aBfSBZjNOrPP9g_XTWEFOqYhVOL78130_head.
- NP662828.RAe7FbvLlKIYiTp_aBfSBZjNOrPP9g_XTWEFOqYhVOL78130_assertion description "[Most patients with GS display the hemophagocytic syndrome and have mutations in RAB27A, which codes for a small GTPase.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP662828.RAe7FbvLlKIYiTp_aBfSBZjNOrPP9g_XTWEFOqYhVOL78130_provenance.
- NP662828.RAe7FbvLlKIYiTp_aBfSBZjNOrPP9g_XTWEFOqYhVOL78130_assertion evidence source_evidence_literature NP662828.RAe7FbvLlKIYiTp_aBfSBZjNOrPP9g_XTWEFOqYhVOL78130_provenance.
- NP662828.RAe7FbvLlKIYiTp_aBfSBZjNOrPP9g_XTWEFOqYhVOL78130_assertion SIO_000772 12058346 NP662828.RAe7FbvLlKIYiTp_aBfSBZjNOrPP9g_XTWEFOqYhVOL78130_provenance.
- NP662828.RAe7FbvLlKIYiTp_aBfSBZjNOrPP9g_XTWEFOqYhVOL78130_assertion wasDerivedFrom befree-20150227 NP662828.RAe7FbvLlKIYiTp_aBfSBZjNOrPP9g_XTWEFOqYhVOL78130_provenance.
- NP662828.RAe7FbvLlKIYiTp_aBfSBZjNOrPP9g_XTWEFOqYhVOL78130_assertion wasGeneratedBy ECO_0000203 NP662828.RAe7FbvLlKIYiTp_aBfSBZjNOrPP9g_XTWEFOqYhVOL78130_provenance.