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- source_evidence_literature type ECO_0000212 NP857466.RATkygLqTd2wLEquMleEpMgzot292AXdt91iH4agi52aU130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP857466.RATkygLqTd2wLEquMleEpMgzot292AXdt91iH4agi52aU130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP857466.RATkygLqTd2wLEquMleEpMgzot292AXdt91iH4agi52aU130_provenance.
- NP857466.RATkygLqTd2wLEquMleEpMgzot292AXdt91iH4agi52aU130_assertion description "[To examine the role of RP1 mutations in RP, we screened 101 unrelated Chinese RP patients (unselected for mode of inheritance) and 190 elderly normal control subjects for sequence changes in the coding exons for the 2156 amino acid RP1 protein.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP857466.RATkygLqTd2wLEquMleEpMgzot292AXdt91iH4agi52aU130_provenance.
- NP857466.RATkygLqTd2wLEquMleEpMgzot292AXdt91iH4agi52aU130_assertion evidence source_evidence_literature NP857466.RATkygLqTd2wLEquMleEpMgzot292AXdt91iH4agi52aU130_provenance.
- NP857466.RATkygLqTd2wLEquMleEpMgzot292AXdt91iH4agi52aU130_assertion SIO_000772 11317367 NP857466.RATkygLqTd2wLEquMleEpMgzot292AXdt91iH4agi52aU130_provenance.
- NP857466.RATkygLqTd2wLEquMleEpMgzot292AXdt91iH4agi52aU130_assertion wasDerivedFrom befree-20150227 NP857466.RATkygLqTd2wLEquMleEpMgzot292AXdt91iH4agi52aU130_provenance.
- NP857466.RATkygLqTd2wLEquMleEpMgzot292AXdt91iH4agi52aU130_assertion wasGeneratedBy ECO_0000203 NP857466.RATkygLqTd2wLEquMleEpMgzot292AXdt91iH4agi52aU130_provenance.
- befree-20150227 importedOn "2015-02-27" NP857466.RATkygLqTd2wLEquMleEpMgzot292AXdt91iH4agi52aU130_provenance.