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- source_evidence_literature type ECO_0000212 NP1108861.RAg9Ib-_HRIRYw6ZUCWbnt2aD-z2Xsxlh-nyamyd4ZJaw130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP1108861.RAg9Ib-_HRIRYw6ZUCWbnt2aD-z2Xsxlh-nyamyd4ZJaw130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP1108861.RAg9Ib-_HRIRYw6ZUCWbnt2aD-z2Xsxlh-nyamyd4ZJaw130_provenance.
- NP1108861.RAg9Ib-_HRIRYw6ZUCWbnt2aD-z2Xsxlh-nyamyd4ZJaw130_assertion description "[Autosomal dominant progressive external ophthalmoplegia due to the p.R357P PEO1 mutation is a late-onset ocular myopathy beginning with ptosis and progressing slowly.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1108861.RAg9Ib-_HRIRYw6ZUCWbnt2aD-z2Xsxlh-nyamyd4ZJaw130_provenance.
- NP1108861.RAg9Ib-_HRIRYw6ZUCWbnt2aD-z2Xsxlh-nyamyd4ZJaw130_assertion evidence source_evidence_literature NP1108861.RAg9Ib-_HRIRYw6ZUCWbnt2aD-z2Xsxlh-nyamyd4ZJaw130_provenance.
- NP1108861.RAg9Ib-_HRIRYw6ZUCWbnt2aD-z2Xsxlh-nyamyd4ZJaw130_assertion SIO_000772 24018892 NP1108861.RAg9Ib-_HRIRYw6ZUCWbnt2aD-z2Xsxlh-nyamyd4ZJaw130_provenance.
- NP1108861.RAg9Ib-_HRIRYw6ZUCWbnt2aD-z2Xsxlh-nyamyd4ZJaw130_assertion wasDerivedFrom befree-2016 NP1108861.RAg9Ib-_HRIRYw6ZUCWbnt2aD-z2Xsxlh-nyamyd4ZJaw130_provenance.
- NP1108861.RAg9Ib-_HRIRYw6ZUCWbnt2aD-z2Xsxlh-nyamyd4ZJaw130_assertion wasGeneratedBy ECO_0000203 NP1108861.RAg9Ib-_HRIRYw6ZUCWbnt2aD-z2Xsxlh-nyamyd4ZJaw130_provenance.
- befree-2016 importedOn "2016-02-19" NP1108861.RAg9Ib-_HRIRYw6ZUCWbnt2aD-z2Xsxlh-nyamyd4ZJaw130_provenance.