Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP1307239.RAoPBfQrPdETOpaLALEaZ7muLM7Zd5I7nYI-Mr7QJLPvU130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP1307239.RAoPBfQrPdETOpaLALEaZ7muLM7Zd5I7nYI-Mr7QJLPvU130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP1307239.RAoPBfQrPdETOpaLALEaZ7muLM7Zd5I7nYI-Mr7QJLPvU130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP1307239.RAoPBfQrPdETOpaLALEaZ7muLM7Zd5I7nYI-Mr7QJLPvU130_provenance.
- NP1307239.RAoPBfQrPdETOpaLALEaZ7muLM7Zd5I7nYI-Mr7QJLPvU130_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." NP1307239.RAoPBfQrPdETOpaLALEaZ7muLM7Zd5I7nYI-Mr7QJLPvU130_provenance.
- NP1307239.RAoPBfQrPdETOpaLALEaZ7muLM7Zd5I7nYI-Mr7QJLPvU130_assertion evidence source_evidence_literature NP1307239.RAoPBfQrPdETOpaLALEaZ7muLM7Zd5I7nYI-Mr7QJLPvU130_provenance.
- NP1307239.RAoPBfQrPdETOpaLALEaZ7muLM7Zd5I7nYI-Mr7QJLPvU130_assertion SIO_000772 6929767 NP1307239.RAoPBfQrPdETOpaLALEaZ7muLM7Zd5I7nYI-Mr7QJLPvU130_provenance.
- NP1307239.RAoPBfQrPdETOpaLALEaZ7muLM7Zd5I7nYI-Mr7QJLPvU130_assertion wasDerivedFrom befree-2016 NP1307239.RAoPBfQrPdETOpaLALEaZ7muLM7Zd5I7nYI-Mr7QJLPvU130_provenance.
- NP1307239.RAoPBfQrPdETOpaLALEaZ7muLM7Zd5I7nYI-Mr7QJLPvU130_assertion wasGeneratedBy ECO_0000203 NP1307239.RAoPBfQrPdETOpaLALEaZ7muLM7Zd5I7nYI-Mr7QJLPvU130_provenance.
- befree-2016 importedOn "2016-02-19" NP1307239.RAoPBfQrPdETOpaLALEaZ7muLM7Zd5I7nYI-Mr7QJLPvU130_provenance.