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- source_evidence_literature type ECO_0000212 NP1357048.RA0biAuJ0Z0lJ1ZN6v_8yBN4qSIOOyKBSFlbIxr8Zfcwc130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP1357048.RA0biAuJ0Z0lJ1ZN6v_8yBN4qSIOOyKBSFlbIxr8Zfcwc130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP1357048.RA0biAuJ0Z0lJ1ZN6v_8yBN4qSIOOyKBSFlbIxr8Zfcwc130_provenance.
- NP1357048.RA0biAuJ0Z0lJ1ZN6v_8yBN4qSIOOyKBSFlbIxr8Zfcwc130_assertion description "[Deficiencies of adhalin in a particular form of limb-girdle muscular dystrophy, and of merosin in a particular form of congenital muscular dystrophy as well as the newly discovered principle of abnormal tri-nucleotide repeats in myotonic dystrophy are evidence of progress that has also amplified the notion of the dystrophinopathies that the protein-deficient muscular dystrophies can now be considered examples of contributions of the dystrophin-glycoprotein complex across the muscle fiber plasma membrane.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1357048.RA0biAuJ0Z0lJ1ZN6v_8yBN4qSIOOyKBSFlbIxr8Zfcwc130_provenance.
- NP1357048.RA0biAuJ0Z0lJ1ZN6v_8yBN4qSIOOyKBSFlbIxr8Zfcwc130_assertion evidence source_evidence_literature NP1357048.RA0biAuJ0Z0lJ1ZN6v_8yBN4qSIOOyKBSFlbIxr8Zfcwc130_provenance.
- NP1357048.RA0biAuJ0Z0lJ1ZN6v_8yBN4qSIOOyKBSFlbIxr8Zfcwc130_assertion SIO_000772 8795845 NP1357048.RA0biAuJ0Z0lJ1ZN6v_8yBN4qSIOOyKBSFlbIxr8Zfcwc130_provenance.
- NP1357048.RA0biAuJ0Z0lJ1ZN6v_8yBN4qSIOOyKBSFlbIxr8Zfcwc130_assertion wasDerivedFrom befree-2016 NP1357048.RA0biAuJ0Z0lJ1ZN6v_8yBN4qSIOOyKBSFlbIxr8Zfcwc130_provenance.
- NP1357048.RA0biAuJ0Z0lJ1ZN6v_8yBN4qSIOOyKBSFlbIxr8Zfcwc130_assertion wasGeneratedBy ECO_0000203 NP1357048.RA0biAuJ0Z0lJ1ZN6v_8yBN4qSIOOyKBSFlbIxr8Zfcwc130_provenance.
- befree-2016 importedOn "2016-02-19" NP1357048.RA0biAuJ0Z0lJ1ZN6v_8yBN4qSIOOyKBSFlbIxr8Zfcwc130_provenance.