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- source_evidence_literature type ECO_0000212 NP77158.RAeDAf1VZ1AgzUImOGDJRlup1fEOe6r6PDi_4lSIM6XHs130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP77158.RAeDAf1VZ1AgzUImOGDJRlup1fEOe6r6PDi_4lSIM6XHs130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP77158.RAeDAf1VZ1AgzUImOGDJRlup1fEOe6r6PDi_4lSIM6XHs130_provenance.
- NP77158.RAeDAf1VZ1AgzUImOGDJRlup1fEOe6r6PDi_4lSIM6XHs130_assertion description "[To our knowledge, this is the first report of successful simultaneous detection of multiple genetic polymorphisms with point mutations using ASPCR-MP or multiple genetic polymorphisms with large structural alterations using stepdown PCR. In conclusion, AS]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP77158.RAeDAf1VZ1AgzUImOGDJRlup1fEOe6r6PDi_4lSIM6XHs130_provenance.
- NP77158.RAeDAf1VZ1AgzUImOGDJRlup1fEOe6r6PDi_4lSIM6XHs130_assertion evidence source_evidence_literature NP77158.RAeDAf1VZ1AgzUImOGDJRlup1fEOe6r6PDi_4lSIM6XHs130_provenance.
- NP77158.RAeDAf1VZ1AgzUImOGDJRlup1fEOe6r6PDi_4lSIM6XHs130_assertion SIO_000772 15691505 NP77158.RAeDAf1VZ1AgzUImOGDJRlup1fEOe6r6PDi_4lSIM6XHs130_provenance.
- NP77158.RAeDAf1VZ1AgzUImOGDJRlup1fEOe6r6PDi_4lSIM6XHs130_assertion wasDerivedFrom gad-20150221 NP77158.RAeDAf1VZ1AgzUImOGDJRlup1fEOe6r6PDi_4lSIM6XHs130_provenance.
- NP77158.RAeDAf1VZ1AgzUImOGDJRlup1fEOe6r6PDi_4lSIM6XHs130_assertion wasGeneratedBy ECO_0000203 NP77158.RAeDAf1VZ1AgzUImOGDJRlup1fEOe6r6PDi_4lSIM6XHs130_provenance.
- gad-20150221 importedOn "2015-02-21" NP77158.RAeDAf1VZ1AgzUImOGDJRlup1fEOe6r6PDi_4lSIM6XHs130_provenance.