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- source_evidence_literature type ECO_0000212 NP919687.RAoO9c7uRdYyWcnkwbmY_keUO2edCkTkF_0EQkRLr07JQ130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP919687.RAoO9c7uRdYyWcnkwbmY_keUO2edCkTkF_0EQkRLr07JQ130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP919687.RAoO9c7uRdYyWcnkwbmY_keUO2edCkTkF_0EQkRLr07JQ130_provenance.
- NP919687.RAoO9c7uRdYyWcnkwbmY_keUO2edCkTkF_0EQkRLr07JQ130_assertion description "[Using a 13-day sequence and analysis pipeline, we discovered direct disruption of CHD7, a causal locus in the CHARGE syndrome (coloboma of the eye, heart anomaly, atresia of the choanae, retardation, and genital and ear anomalies).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP919687.RAoO9c7uRdYyWcnkwbmY_keUO2edCkTkF_0EQkRLr07JQ130_provenance.
- NP919687.RAoO9c7uRdYyWcnkwbmY_keUO2edCkTkF_0EQkRLr07JQ130_assertion evidence source_evidence_literature NP919687.RAoO9c7uRdYyWcnkwbmY_keUO2edCkTkF_0EQkRLr07JQ130_provenance.
- NP919687.RAoO9c7uRdYyWcnkwbmY_keUO2edCkTkF_0EQkRLr07JQ130_assertion SIO_000772 23215558 NP919687.RAoO9c7uRdYyWcnkwbmY_keUO2edCkTkF_0EQkRLr07JQ130_provenance.
- NP919687.RAoO9c7uRdYyWcnkwbmY_keUO2edCkTkF_0EQkRLr07JQ130_assertion wasDerivedFrom befree-20150227 NP919687.RAoO9c7uRdYyWcnkwbmY_keUO2edCkTkF_0EQkRLr07JQ130_provenance.
- NP919687.RAoO9c7uRdYyWcnkwbmY_keUO2edCkTkF_0EQkRLr07JQ130_assertion wasGeneratedBy ECO_0000203 NP919687.RAoO9c7uRdYyWcnkwbmY_keUO2edCkTkF_0EQkRLr07JQ130_provenance.
- befree-20150227 importedOn "2015-02-27" NP919687.RAoO9c7uRdYyWcnkwbmY_keUO2edCkTkF_0EQkRLr07JQ130_provenance.