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- source_evidence_literature type ECO_0000212 NP237616.RA1foc0Qdvi8WlNnbcRg9th_eAWMtAFpyBF1Z0Eia22xo130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP237616.RA1foc0Qdvi8WlNnbcRg9th_eAWMtAFpyBF1Z0Eia22xo130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP237616.RA1foc0Qdvi8WlNnbcRg9th_eAWMtAFpyBF1Z0Eia22xo130_provenance.
- NP237616.RA1foc0Qdvi8WlNnbcRg9th_eAWMtAFpyBF1Z0Eia22xo130_assertion description "[In summary, heterozigosity for the C34T allele of the AMPD gene is associated with reduced submaximal aerobic capacity in female patients with McArdle disease and might partly account, in this gender, for the variability that exists in the phenotypic manifestation of the disease.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP237616.RA1foc0Qdvi8WlNnbcRg9th_eAWMtAFpyBF1Z0Eia22xo130_provenance.
- NP237616.RA1foc0Qdvi8WlNnbcRg9th_eAWMtAFpyBF1Z0Eia22xo130_assertion evidence source_evidence_literature NP237616.RA1foc0Qdvi8WlNnbcRg9th_eAWMtAFpyBF1Z0Eia22xo130_provenance.
- NP237616.RA1foc0Qdvi8WlNnbcRg9th_eAWMtAFpyBF1Z0Eia22xo130_assertion SIO_000772 17687759 NP237616.RA1foc0Qdvi8WlNnbcRg9th_eAWMtAFpyBF1Z0Eia22xo130_provenance.
- NP237616.RA1foc0Qdvi8WlNnbcRg9th_eAWMtAFpyBF1Z0Eia22xo130_assertion wasDerivedFrom befree-20150227 NP237616.RA1foc0Qdvi8WlNnbcRg9th_eAWMtAFpyBF1Z0Eia22xo130_provenance.
- NP237616.RA1foc0Qdvi8WlNnbcRg9th_eAWMtAFpyBF1Z0Eia22xo130_assertion wasGeneratedBy ECO_0000203 NP237616.RA1foc0Qdvi8WlNnbcRg9th_eAWMtAFpyBF1Z0Eia22xo130_provenance.
- befree-20150227 importedOn "2015-02-27" NP237616.RA1foc0Qdvi8WlNnbcRg9th_eAWMtAFpyBF1Z0Eia22xo130_provenance.