Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP209080.RAToS4A0alDD4Eq6i01CxlFqR6WYMoVD0AMWci5pcKNmE130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP209080.RAToS4A0alDD4Eq6i01CxlFqR6WYMoVD0AMWci5pcKNmE130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP209080.RAToS4A0alDD4Eq6i01CxlFqR6WYMoVD0AMWci5pcKNmE130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP209080.RAToS4A0alDD4Eq6i01CxlFqR6WYMoVD0AMWci5pcKNmE130_provenance.
- NP209080.RAToS4A0alDD4Eq6i01CxlFqR6WYMoVD0AMWci5pcKNmE130_assertion description "[ACTN4 mutations accounts for about 3.5% of familial focal glomerulosclerosis.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP209080.RAToS4A0alDD4Eq6i01CxlFqR6WYMoVD0AMWci5pcKNmE130_provenance.
- NP209080.RAToS4A0alDD4Eq6i01CxlFqR6WYMoVD0AMWci5pcKNmE130_assertion evidence source_evidence_literature NP209080.RAToS4A0alDD4Eq6i01CxlFqR6WYMoVD0AMWci5pcKNmE130_provenance.
- NP209080.RAToS4A0alDD4Eq6i01CxlFqR6WYMoVD0AMWci5pcKNmE130_assertion SIO_000772 16251236 NP209080.RAToS4A0alDD4Eq6i01CxlFqR6WYMoVD0AMWci5pcKNmE130_provenance.
- NP209080.RAToS4A0alDD4Eq6i01CxlFqR6WYMoVD0AMWci5pcKNmE130_assertion wasDerivedFrom lhgdn-20090331 NP209080.RAToS4A0alDD4Eq6i01CxlFqR6WYMoVD0AMWci5pcKNmE130_provenance.
- NP209080.RAToS4A0alDD4Eq6i01CxlFqR6WYMoVD0AMWci5pcKNmE130_assertion wasGeneratedBy ECO_0000203 NP209080.RAToS4A0alDD4Eq6i01CxlFqR6WYMoVD0AMWci5pcKNmE130_provenance.
- lhgdn-20090331 importedOn "2009-03-31" NP209080.RAToS4A0alDD4Eq6i01CxlFqR6WYMoVD0AMWci5pcKNmE130_provenance.