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- source_evidence_literature type ECO_0000212 NP676882.RAbAvi7Qr6sF20t2Ls8c6gSVqt2Ikz1Iwa_2A6jZKr9tE130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP676882.RAbAvi7Qr6sF20t2Ls8c6gSVqt2Ikz1Iwa_2A6jZKr9tE130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP676882.RAbAvi7Qr6sF20t2Ls8c6gSVqt2Ikz1Iwa_2A6jZKr9tE130_provenance.
- befree-20150227 importedOn "2015-02-27" NP676882.RAbAvi7Qr6sF20t2Ls8c6gSVqt2Ikz1Iwa_2A6jZKr9tE130_provenance.
- NP676882.RAbAvi7Qr6sF20t2Ls8c6gSVqt2Ikz1Iwa_2A6jZKr9tE130_assertion wasGeneratedBy ECO_0000203 NP676882.RAbAvi7Qr6sF20t2Ls8c6gSVqt2Ikz1Iwa_2A6jZKr9tE130_provenance.
- NP676882.RAbAvi7Qr6sF20t2Ls8c6gSVqt2Ikz1Iwa_2A6jZKr9tE130_assertion wasDerivedFrom befree-20150227 NP676882.RAbAvi7Qr6sF20t2Ls8c6gSVqt2Ikz1Iwa_2A6jZKr9tE130_provenance.
- NP676882.RAbAvi7Qr6sF20t2Ls8c6gSVqt2Ikz1Iwa_2A6jZKr9tE130_assertion SIO_000772 24091937 NP676882.RAbAvi7Qr6sF20t2Ls8c6gSVqt2Ikz1Iwa_2A6jZKr9tE130_provenance.
- NP676882.RAbAvi7Qr6sF20t2Ls8c6gSVqt2Ikz1Iwa_2A6jZKr9tE130_assertion evidence source_evidence_literature NP676882.RAbAvi7Qr6sF20t2Ls8c6gSVqt2Ikz1Iwa_2A6jZKr9tE130_provenance.
- NP676882.RAbAvi7Qr6sF20t2Ls8c6gSVqt2Ikz1Iwa_2A6jZKr9tE130_assertion description "[RYR1-associated myopathies should be included in the differential diagnosis of congenital ophthalmoplegia and facial weakness, even without clinical skeletal myopathy.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP676882.RAbAvi7Qr6sF20t2Ls8c6gSVqt2Ikz1Iwa_2A6jZKr9tE130_provenance.