Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP496369.RASd_Ee_3CIPSKFN9C_b26r9ixN8S0trtcmTr18BSNvr4130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP496369.RASd_Ee_3CIPSKFN9C_b26r9ixN8S0trtcmTr18BSNvr4130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP496369.RASd_Ee_3CIPSKFN9C_b26r9ixN8S0trtcmTr18BSNvr4130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP496369.RASd_Ee_3CIPSKFN9C_b26r9ixN8S0trtcmTr18BSNvr4130_provenance.
- NP496369.RASd_Ee_3CIPSKFN9C_b26r9ixN8S0trtcmTr18BSNvr4130_assertion description "[We suggest that the absence of the ZDHHC15 transcripts in this patient contributes to her phenotype, and that the gene is a strong candidate for nonsyndromic XLMR.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP496369.RASd_Ee_3CIPSKFN9C_b26r9ixN8S0trtcmTr18BSNvr4130_provenance.
- NP496369.RASd_Ee_3CIPSKFN9C_b26r9ixN8S0trtcmTr18BSNvr4130_assertion evidence source_evidence_literature NP496369.RASd_Ee_3CIPSKFN9C_b26r9ixN8S0trtcmTr18BSNvr4130_provenance.
- NP496369.RASd_Ee_3CIPSKFN9C_b26r9ixN8S0trtcmTr18BSNvr4130_assertion SIO_000772 15915161 NP496369.RASd_Ee_3CIPSKFN9C_b26r9ixN8S0trtcmTr18BSNvr4130_provenance.
- NP496369.RASd_Ee_3CIPSKFN9C_b26r9ixN8S0trtcmTr18BSNvr4130_assertion wasDerivedFrom befree-2016 NP496369.RASd_Ee_3CIPSKFN9C_b26r9ixN8S0trtcmTr18BSNvr4130_provenance.
- NP496369.RASd_Ee_3CIPSKFN9C_b26r9ixN8S0trtcmTr18BSNvr4130_assertion wasGeneratedBy ECO_0000203 NP496369.RASd_Ee_3CIPSKFN9C_b26r9ixN8S0trtcmTr18BSNvr4130_provenance.
- befree-2016 importedOn "2016-02-19" NP496369.RASd_Ee_3CIPSKFN9C_b26r9ixN8S0trtcmTr18BSNvr4130_provenance.