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- source_evidence_literature type ECO_0000212 NP442514.RATJsmyq6FfbNoEffZF0ccOQWaauk9Ux9O_HZSbemuZT0130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP442514.RATJsmyq6FfbNoEffZF0ccOQWaauk9Ux9O_HZSbemuZT0130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP442514.RATJsmyq6FfbNoEffZF0ccOQWaauk9Ux9O_HZSbemuZT0130_provenance.
- NP442514.RATJsmyq6FfbNoEffZF0ccOQWaauk9Ux9O_HZSbemuZT0130_assertion description "[A novel GUCY2D mutation in a Chinese family with dominant cone dystrophy.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP442514.RATJsmyq6FfbNoEffZF0ccOQWaauk9Ux9O_HZSbemuZT0130_provenance.
- NP442514.RATJsmyq6FfbNoEffZF0ccOQWaauk9Ux9O_HZSbemuZT0130_assertion evidence source_evidence_literature NP442514.RATJsmyq6FfbNoEffZF0ccOQWaauk9Ux9O_HZSbemuZT0130_provenance.
- NP442514.RATJsmyq6FfbNoEffZF0ccOQWaauk9Ux9O_HZSbemuZT0130_assertion SIO_000772 23734073 NP442514.RATJsmyq6FfbNoEffZF0ccOQWaauk9Ux9O_HZSbemuZT0130_provenance.
- NP442514.RATJsmyq6FfbNoEffZF0ccOQWaauk9Ux9O_HZSbemuZT0130_assertion wasDerivedFrom befree-20150227 NP442514.RATJsmyq6FfbNoEffZF0ccOQWaauk9Ux9O_HZSbemuZT0130_provenance.
- NP442514.RATJsmyq6FfbNoEffZF0ccOQWaauk9Ux9O_HZSbemuZT0130_assertion wasGeneratedBy ECO_0000203 NP442514.RATJsmyq6FfbNoEffZF0ccOQWaauk9Ux9O_HZSbemuZT0130_provenance.
- befree-20150227 importedOn "2015-02-27" NP442514.RATJsmyq6FfbNoEffZF0ccOQWaauk9Ux9O_HZSbemuZT0130_provenance.