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- source_evidence_literature type ECO_0000212 NP1027482.RAHJAs5wbvvN2UqlIfiAShvwebr6riXYV8BmRBghiXfkk130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP1027482.RAHJAs5wbvvN2UqlIfiAShvwebr6riXYV8BmRBghiXfkk130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP1027482.RAHJAs5wbvvN2UqlIfiAShvwebr6riXYV8BmRBghiXfkk130_provenance.
- NP1027482.RAHJAs5wbvvN2UqlIfiAShvwebr6riXYV8BmRBghiXfkk130_assertion description "[Mutations of the lamin A/C gene are associated with several different neuromuscular diseases, and the detailed effect of disease-associated amino acid substitutions on the structure and stability of human lamin dimers is yet unknown.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1027482.RAHJAs5wbvvN2UqlIfiAShvwebr6riXYV8BmRBghiXfkk130_provenance.
- NP1027482.RAHJAs5wbvvN2UqlIfiAShvwebr6riXYV8BmRBghiXfkk130_assertion evidence source_evidence_literature NP1027482.RAHJAs5wbvvN2UqlIfiAShvwebr6riXYV8BmRBghiXfkk130_provenance.
- NP1027482.RAHJAs5wbvvN2UqlIfiAShvwebr6riXYV8BmRBghiXfkk130_assertion SIO_000772 23142632 NP1027482.RAHJAs5wbvvN2UqlIfiAShvwebr6riXYV8BmRBghiXfkk130_provenance.
- NP1027482.RAHJAs5wbvvN2UqlIfiAShvwebr6riXYV8BmRBghiXfkk130_assertion wasDerivedFrom befree-2016 NP1027482.RAHJAs5wbvvN2UqlIfiAShvwebr6riXYV8BmRBghiXfkk130_provenance.
- NP1027482.RAHJAs5wbvvN2UqlIfiAShvwebr6riXYV8BmRBghiXfkk130_assertion wasGeneratedBy ECO_0000203 NP1027482.RAHJAs5wbvvN2UqlIfiAShvwebr6riXYV8BmRBghiXfkk130_provenance.
- befree-2016 importedOn "2016-02-19" NP1027482.RAHJAs5wbvvN2UqlIfiAShvwebr6riXYV8BmRBghiXfkk130_provenance.