Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP614599.RAG9i6t70LHfLjZLWfT6KhfJvQKUipp8XCCIVdtj88vGY130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP614599.RAG9i6t70LHfLjZLWfT6KhfJvQKUipp8XCCIVdtj88vGY130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP614599.RAG9i6t70LHfLjZLWfT6KhfJvQKUipp8XCCIVdtj88vGY130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP614599.RAG9i6t70LHfLjZLWfT6KhfJvQKUipp8XCCIVdtj88vGY130_provenance.
- NP614599.RAG9i6t70LHfLjZLWfT6KhfJvQKUipp8XCCIVdtj88vGY130_assertion description "[Defects in the newly reported gene NPHS1 in chromosome 19 cause the massive proteinuria of Finnish type congenital nephrotic syndrome (CNF).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP614599.RAG9i6t70LHfLjZLWfT6KhfJvQKUipp8XCCIVdtj88vGY130_provenance.
- NP614599.RAG9i6t70LHfLjZLWfT6KhfJvQKUipp8XCCIVdtj88vGY130_assertion evidence source_evidence_literature NP614599.RAG9i6t70LHfLjZLWfT6KhfJvQKUipp8XCCIVdtj88vGY130_provenance.
- NP614599.RAG9i6t70LHfLjZLWfT6KhfJvQKUipp8XCCIVdtj88vGY130_assertion SIO_000772 10550324 NP614599.RAG9i6t70LHfLjZLWfT6KhfJvQKUipp8XCCIVdtj88vGY130_provenance.
- NP614599.RAG9i6t70LHfLjZLWfT6KhfJvQKUipp8XCCIVdtj88vGY130_assertion wasDerivedFrom befree-20140225 NP614599.RAG9i6t70LHfLjZLWfT6KhfJvQKUipp8XCCIVdtj88vGY130_provenance.
- NP614599.RAG9i6t70LHfLjZLWfT6KhfJvQKUipp8XCCIVdtj88vGY130_assertion wasGeneratedBy ECO_0000203 NP614599.RAG9i6t70LHfLjZLWfT6KhfJvQKUipp8XCCIVdtj88vGY130_provenance.
- befree-20140225 importedOn "2014-02-25" NP614599.RAG9i6t70LHfLjZLWfT6KhfJvQKUipp8XCCIVdtj88vGY130_provenance.