Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP431007.RAN8hWw_oRBgQLZ2YXKaoGH_KLjIwhGwkMFTmE9WsXZtw130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP431007.RAN8hWw_oRBgQLZ2YXKaoGH_KLjIwhGwkMFTmE9WsXZtw130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP431007.RAN8hWw_oRBgQLZ2YXKaoGH_KLjIwhGwkMFTmE9WsXZtw130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP431007.RAN8hWw_oRBgQLZ2YXKaoGH_KLjIwhGwkMFTmE9WsXZtw130_provenance.
- befree-20150227 importedOn "2015-02-27" NP431007.RAN8hWw_oRBgQLZ2YXKaoGH_KLjIwhGwkMFTmE9WsXZtw130_provenance.
- NP431007.RAN8hWw_oRBgQLZ2YXKaoGH_KLjIwhGwkMFTmE9WsXZtw130_assertion wasGeneratedBy ECO_0000203 NP431007.RAN8hWw_oRBgQLZ2YXKaoGH_KLjIwhGwkMFTmE9WsXZtw130_provenance.
- NP431007.RAN8hWw_oRBgQLZ2YXKaoGH_KLjIwhGwkMFTmE9WsXZtw130_assertion wasDerivedFrom befree-20150227 NP431007.RAN8hWw_oRBgQLZ2YXKaoGH_KLjIwhGwkMFTmE9WsXZtw130_provenance.
- NP431007.RAN8hWw_oRBgQLZ2YXKaoGH_KLjIwhGwkMFTmE9WsXZtw130_assertion SIO_000772 10814714 NP431007.RAN8hWw_oRBgQLZ2YXKaoGH_KLjIwhGwkMFTmE9WsXZtw130_provenance.
- NP431007.RAN8hWw_oRBgQLZ2YXKaoGH_KLjIwhGwkMFTmE9WsXZtw130_assertion evidence source_evidence_literature NP431007.RAN8hWw_oRBgQLZ2YXKaoGH_KLjIwhGwkMFTmE9WsXZtw130_provenance.
- NP431007.RAN8hWw_oRBgQLZ2YXKaoGH_KLjIwhGwkMFTmE9WsXZtw130_assertion description "[Mutational analysis of the GPC3/GPC4 glypican gene cluster on Xq26 in patients with Simpson-Golabi-Behmel syndrome: identification of loss-of-function mutations in the GPC3 gene.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP431007.RAN8hWw_oRBgQLZ2YXKaoGH_KLjIwhGwkMFTmE9WsXZtw130_provenance.