Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP267230.RAVdzipOAREhP36ORlU5faoLDpgCDwccjJoUwrFqPEQrY130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP267230.RAVdzipOAREhP36ORlU5faoLDpgCDwccjJoUwrFqPEQrY130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP267230.RAVdzipOAREhP36ORlU5faoLDpgCDwccjJoUwrFqPEQrY130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP267230.RAVdzipOAREhP36ORlU5faoLDpgCDwccjJoUwrFqPEQrY130_provenance.
- NP267230.RAVdzipOAREhP36ORlU5faoLDpgCDwccjJoUwrFqPEQrY130_assertion description "[We found the rare properdin factor B(Bf) variant F1 to be present in 11% of 72 patients suffering from insulin-dependent diabetes (IDDM) compared with 2% among 150 normal controls.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP267230.RAVdzipOAREhP36ORlU5faoLDpgCDwccjJoUwrFqPEQrY130_provenance.
- NP267230.RAVdzipOAREhP36ORlU5faoLDpgCDwccjJoUwrFqPEQrY130_assertion evidence source_evidence_literature NP267230.RAVdzipOAREhP36ORlU5faoLDpgCDwccjJoUwrFqPEQrY130_provenance.
- NP267230.RAVdzipOAREhP36ORlU5faoLDpgCDwccjJoUwrFqPEQrY130_assertion SIO_000772 6929767 NP267230.RAVdzipOAREhP36ORlU5faoLDpgCDwccjJoUwrFqPEQrY130_provenance.
- NP267230.RAVdzipOAREhP36ORlU5faoLDpgCDwccjJoUwrFqPEQrY130_assertion wasDerivedFrom befree-20150227 NP267230.RAVdzipOAREhP36ORlU5faoLDpgCDwccjJoUwrFqPEQrY130_provenance.
- NP267230.RAVdzipOAREhP36ORlU5faoLDpgCDwccjJoUwrFqPEQrY130_assertion wasGeneratedBy ECO_0000203 NP267230.RAVdzipOAREhP36ORlU5faoLDpgCDwccjJoUwrFqPEQrY130_provenance.
- befree-20150227 importedOn "2015-02-27" NP267230.RAVdzipOAREhP36ORlU5faoLDpgCDwccjJoUwrFqPEQrY130_provenance.