Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP923781.RAFW2BZsDxDTvlFYPEDVVCD-MXIeXF82UpjUNsR4GcXt4130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP923781.RAFW2BZsDxDTvlFYPEDVVCD-MXIeXF82UpjUNsR4GcXt4130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP923781.RAFW2BZsDxDTvlFYPEDVVCD-MXIeXF82UpjUNsR4GcXt4130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP923781.RAFW2BZsDxDTvlFYPEDVVCD-MXIeXF82UpjUNsR4GcXt4130_provenance.
- NP923781.RAFW2BZsDxDTvlFYPEDVVCD-MXIeXF82UpjUNsR4GcXt4130_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." NP923781.RAFW2BZsDxDTvlFYPEDVVCD-MXIeXF82UpjUNsR4GcXt4130_provenance.
- NP923781.RAFW2BZsDxDTvlFYPEDVVCD-MXIeXF82UpjUNsR4GcXt4130_assertion evidence source_evidence_literature NP923781.RAFW2BZsDxDTvlFYPEDVVCD-MXIeXF82UpjUNsR4GcXt4130_provenance.
- NP923781.RAFW2BZsDxDTvlFYPEDVVCD-MXIeXF82UpjUNsR4GcXt4130_assertion SIO_000772 24018892 NP923781.RAFW2BZsDxDTvlFYPEDVVCD-MXIeXF82UpjUNsR4GcXt4130_provenance.
- NP923781.RAFW2BZsDxDTvlFYPEDVVCD-MXIeXF82UpjUNsR4GcXt4130_assertion wasDerivedFrom befree-20150227 NP923781.RAFW2BZsDxDTvlFYPEDVVCD-MXIeXF82UpjUNsR4GcXt4130_provenance.
- NP923781.RAFW2BZsDxDTvlFYPEDVVCD-MXIeXF82UpjUNsR4GcXt4130_assertion wasGeneratedBy ECO_0000203 NP923781.RAFW2BZsDxDTvlFYPEDVVCD-MXIeXF82UpjUNsR4GcXt4130_provenance.
- befree-20150227 importedOn "2015-02-27" NP923781.RAFW2BZsDxDTvlFYPEDVVCD-MXIeXF82UpjUNsR4GcXt4130_provenance.