Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP662828.RAe7FbvLlKIYiTp_aBfSBZjNOrPP9g_XTWEFOqYhVOL78130_provenance>. }
Showing items 1 to 9 of
9
with 100 items per page.
- source_evidence_literature type ECO_0000212 NP662828.RAe7FbvLlKIYiTp_aBfSBZjNOrPP9g_XTWEFOqYhVOL78130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP662828.RAe7FbvLlKIYiTp_aBfSBZjNOrPP9g_XTWEFOqYhVOL78130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP662828.RAe7FbvLlKIYiTp_aBfSBZjNOrPP9g_XTWEFOqYhVOL78130_provenance.
- 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.
- befree-20150227 importedOn "2015-02-27" NP662828.RAe7FbvLlKIYiTp_aBfSBZjNOrPP9g_XTWEFOqYhVOL78130_provenance.