Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP576589.RAEL0RG5Z7eCyAcm6Hvje-UmtaJVwbpuD2_dLhuXgwd64130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP576589.RAEL0RG5Z7eCyAcm6Hvje-UmtaJVwbpuD2_dLhuXgwd64130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP576589.RAEL0RG5Z7eCyAcm6Hvje-UmtaJVwbpuD2_dLhuXgwd64130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP576589.RAEL0RG5Z7eCyAcm6Hvje-UmtaJVwbpuD2_dLhuXgwd64130_provenance.
- befree-20150227 importedOn "2015-02-27" NP576589.RAEL0RG5Z7eCyAcm6Hvje-UmtaJVwbpuD2_dLhuXgwd64130_provenance.
- NP576589.RAEL0RG5Z7eCyAcm6Hvje-UmtaJVwbpuD2_dLhuXgwd64130_assertion wasGeneratedBy ECO_0000203 NP576589.RAEL0RG5Z7eCyAcm6Hvje-UmtaJVwbpuD2_dLhuXgwd64130_provenance.
- NP576589.RAEL0RG5Z7eCyAcm6Hvje-UmtaJVwbpuD2_dLhuXgwd64130_assertion wasDerivedFrom befree-20150227 NP576589.RAEL0RG5Z7eCyAcm6Hvje-UmtaJVwbpuD2_dLhuXgwd64130_provenance.
- NP576589.RAEL0RG5Z7eCyAcm6Hvje-UmtaJVwbpuD2_dLhuXgwd64130_assertion SIO_000772 20357205 NP576589.RAEL0RG5Z7eCyAcm6Hvje-UmtaJVwbpuD2_dLhuXgwd64130_provenance.
- NP576589.RAEL0RG5Z7eCyAcm6Hvje-UmtaJVwbpuD2_dLhuXgwd64130_assertion evidence source_evidence_literature NP576589.RAEL0RG5Z7eCyAcm6Hvje-UmtaJVwbpuD2_dLhuXgwd64130_provenance.
- NP576589.RAEL0RG5Z7eCyAcm6Hvje-UmtaJVwbpuD2_dLhuXgwd64130_assertion description "[Common mutations for Leber's hereditary optic neuropathy (LHON: G11778A; T14484C; and G3460A) were not present in AMD samples.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP576589.RAEL0RG5Z7eCyAcm6Hvje-UmtaJVwbpuD2_dLhuXgwd64130_provenance.