Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP230807.RAc3U0p6oIIYKCeAClvRv_e6NHgyllL3Lk93a8f_PbbUA130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP230807.RAc3U0p6oIIYKCeAClvRv_e6NHgyllL3Lk93a8f_PbbUA130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP230807.RAc3U0p6oIIYKCeAClvRv_e6NHgyllL3Lk93a8f_PbbUA130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP230807.RAc3U0p6oIIYKCeAClvRv_e6NHgyllL3Lk93a8f_PbbUA130_provenance.
- NP230807.RAc3U0p6oIIYKCeAClvRv_e6NHgyllL3Lk93a8f_PbbUA130_assertion description "[Heterozygous R1215Q mutation is found in atypical hemolytic uremic syndrome, with incomplete penetrance of the disease.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP230807.RAc3U0p6oIIYKCeAClvRv_e6NHgyllL3Lk93a8f_PbbUA130_provenance.
- NP230807.RAc3U0p6oIIYKCeAClvRv_e6NHgyllL3Lk93a8f_PbbUA130_assertion evidence source_evidence_literature NP230807.RAc3U0p6oIIYKCeAClvRv_e6NHgyllL3Lk93a8f_PbbUA130_provenance.
- NP230807.RAc3U0p6oIIYKCeAClvRv_e6NHgyllL3Lk93a8f_PbbUA130_assertion SIO_000772 17973958 NP230807.RAc3U0p6oIIYKCeAClvRv_e6NHgyllL3Lk93a8f_PbbUA130_provenance.
- NP230807.RAc3U0p6oIIYKCeAClvRv_e6NHgyllL3Lk93a8f_PbbUA130_assertion wasDerivedFrom lhgdn-20090331 NP230807.RAc3U0p6oIIYKCeAClvRv_e6NHgyllL3Lk93a8f_PbbUA130_provenance.
- NP230807.RAc3U0p6oIIYKCeAClvRv_e6NHgyllL3Lk93a8f_PbbUA130_assertion wasGeneratedBy ECO_0000203 NP230807.RAc3U0p6oIIYKCeAClvRv_e6NHgyllL3Lk93a8f_PbbUA130_provenance.
- lhgdn-20090331 importedOn "2009-03-31" NP230807.RAc3U0p6oIIYKCeAClvRv_e6NHgyllL3Lk93a8f_PbbUA130_provenance.