Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP651568.RAM1F2Ka0JaW2Vfphonr6IsqkM-3ZubQisQgNTgD7Y6T4130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP651568.RAM1F2Ka0JaW2Vfphonr6IsqkM-3ZubQisQgNTgD7Y6T4130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP651568.RAM1F2Ka0JaW2Vfphonr6IsqkM-3ZubQisQgNTgD7Y6T4130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP651568.RAM1F2Ka0JaW2Vfphonr6IsqkM-3ZubQisQgNTgD7Y6T4130_provenance.
- NP651568.RAM1F2Ka0JaW2Vfphonr6IsqkM-3ZubQisQgNTgD7Y6T4130_assertion description "[The most severe prognosis was in the CFH mutation group, 60% of whom reached ESRD or died within <1 yr. Only 30% of CFH mutations were localized in SCR20.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP651568.RAM1F2Ka0JaW2Vfphonr6IsqkM-3ZubQisQgNTgD7Y6T4130_provenance.
- NP651568.RAM1F2Ka0JaW2Vfphonr6IsqkM-3ZubQisQgNTgD7Y6T4130_assertion evidence source_evidence_literature NP651568.RAM1F2Ka0JaW2Vfphonr6IsqkM-3ZubQisQgNTgD7Y6T4130_provenance.
- NP651568.RAM1F2Ka0JaW2Vfphonr6IsqkM-3ZubQisQgNTgD7Y6T4130_assertion SIO_000772 17599974 NP651568.RAM1F2Ka0JaW2Vfphonr6IsqkM-3ZubQisQgNTgD7Y6T4130_provenance.
- NP651568.RAM1F2Ka0JaW2Vfphonr6IsqkM-3ZubQisQgNTgD7Y6T4130_assertion wasDerivedFrom befree-20140225 NP651568.RAM1F2Ka0JaW2Vfphonr6IsqkM-3ZubQisQgNTgD7Y6T4130_provenance.
- NP651568.RAM1F2Ka0JaW2Vfphonr6IsqkM-3ZubQisQgNTgD7Y6T4130_assertion wasGeneratedBy ECO_0000203 NP651568.RAM1F2Ka0JaW2Vfphonr6IsqkM-3ZubQisQgNTgD7Y6T4130_provenance.
- befree-20140225 importedOn "2014-02-25" NP651568.RAM1F2Ka0JaW2Vfphonr6IsqkM-3ZubQisQgNTgD7Y6T4130_provenance.