Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP617297.RAV9FHH-3N8W2yxR8KcXdckRFmhoyhWkPv_JDlxz8_qEQ130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP617297.RAV9FHH-3N8W2yxR8KcXdckRFmhoyhWkPv_JDlxz8_qEQ130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP617297.RAV9FHH-3N8W2yxR8KcXdckRFmhoyhWkPv_JDlxz8_qEQ130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP617297.RAV9FHH-3N8W2yxR8KcXdckRFmhoyhWkPv_JDlxz8_qEQ130_provenance.
- NP617297.RAV9FHH-3N8W2yxR8KcXdckRFmhoyhWkPv_JDlxz8_qEQ130_assertion wasGeneratedBy ECO_0000203 NP617297.RAV9FHH-3N8W2yxR8KcXdckRFmhoyhWkPv_JDlxz8_qEQ130_provenance.
- NP617297.RAV9FHH-3N8W2yxR8KcXdckRFmhoyhWkPv_JDlxz8_qEQ130_assertion wasDerivedFrom befree-20140225 NP617297.RAV9FHH-3N8W2yxR8KcXdckRFmhoyhWkPv_JDlxz8_qEQ130_provenance.
- NP617297.RAV9FHH-3N8W2yxR8KcXdckRFmhoyhWkPv_JDlxz8_qEQ130_assertion SIO_000772 16708387 NP617297.RAV9FHH-3N8W2yxR8KcXdckRFmhoyhWkPv_JDlxz8_qEQ130_provenance.
- NP617297.RAV9FHH-3N8W2yxR8KcXdckRFmhoyhWkPv_JDlxz8_qEQ130_assertion evidence source_evidence_literature NP617297.RAV9FHH-3N8W2yxR8KcXdckRFmhoyhWkPv_JDlxz8_qEQ130_provenance.
- NP617297.RAV9FHH-3N8W2yxR8KcXdckRFmhoyhWkPv_JDlxz8_qEQ130_assertion description "[Variation in retinitis pigmentosa-11 (PRPF31 or RP11) gene expression between symptomatic and asymptomatic patients with dominant RP11 mutations.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP617297.RAV9FHH-3N8W2yxR8KcXdckRFmhoyhWkPv_JDlxz8_qEQ130_provenance.
- befree-20140225 importedOn "2014-02-25" NP617297.RAV9FHH-3N8W2yxR8KcXdckRFmhoyhWkPv_JDlxz8_qEQ130_provenance.