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- source_evidence_literature type ECO_0000212 NP665547.RA_Nng-uDxQfHRN-XHENGu_ApeEuG-Eh34gPmimOCr6lQ130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP665547.RA_Nng-uDxQfHRN-XHENGu_ApeEuG-Eh34gPmimOCr6lQ130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP665547.RA_Nng-uDxQfHRN-XHENGu_ApeEuG-Eh34gPmimOCr6lQ130_provenance.
- NP665547.RA_Nng-uDxQfHRN-XHENGu_ApeEuG-Eh34gPmimOCr6lQ130_assertion wasGeneratedBy ECO_0000203 NP665547.RA_Nng-uDxQfHRN-XHENGu_ApeEuG-Eh34gPmimOCr6lQ130_provenance.
- NP665547.RA_Nng-uDxQfHRN-XHENGu_ApeEuG-Eh34gPmimOCr6lQ130_assertion wasDerivedFrom befree-20140225 NP665547.RA_Nng-uDxQfHRN-XHENGu_ApeEuG-Eh34gPmimOCr6lQ130_provenance.
- NP665547.RA_Nng-uDxQfHRN-XHENGu_ApeEuG-Eh34gPmimOCr6lQ130_assertion SIO_000772 20234391 NP665547.RA_Nng-uDxQfHRN-XHENGu_ApeEuG-Eh34gPmimOCr6lQ130_provenance.
- NP665547.RA_Nng-uDxQfHRN-XHENGu_ApeEuG-Eh34gPmimOCr6lQ130_assertion evidence source_evidence_literature NP665547.RA_Nng-uDxQfHRN-XHENGu_ApeEuG-Eh34gPmimOCr6lQ130_provenance.
- NP665547.RA_Nng-uDxQfHRN-XHENGu_ApeEuG-Eh34gPmimOCr6lQ130_assertion description "[Heterozygous deletion of a 2-Mb region including the dystroglycan gene in a patient with mild myopathy, facial hypotonia, oral-motor dyspraxia and white matter abnormalities.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP665547.RA_Nng-uDxQfHRN-XHENGu_ApeEuG-Eh34gPmimOCr6lQ130_provenance.
- befree-20140225 importedOn "2014-02-25" NP665547.RA_Nng-uDxQfHRN-XHENGu_ApeEuG-Eh34gPmimOCr6lQ130_provenance.