Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP518783.RA0qaztfKgkJgW3wtQF679UITSqy4opOWwlb1DDb8lQrg130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP518783.RA0qaztfKgkJgW3wtQF679UITSqy4opOWwlb1DDb8lQrg130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP518783.RA0qaztfKgkJgW3wtQF679UITSqy4opOWwlb1DDb8lQrg130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP518783.RA0qaztfKgkJgW3wtQF679UITSqy4opOWwlb1DDb8lQrg130_provenance.
- NP518783.RA0qaztfKgkJgW3wtQF679UITSqy4opOWwlb1DDb8lQrg130_assertion description "[Clinical data of ten patients and brain MRI (available for six) showed that the phenotype substantially overlapped known SCA15 cases,but we also noted buccolingual dyskinesias, facial myokymias,and pyramidal signs never reported in SCA15.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP518783.RA0qaztfKgkJgW3wtQF679UITSqy4opOWwlb1DDb8lQrg130_provenance.
- NP518783.RA0qaztfKgkJgW3wtQF679UITSqy4opOWwlb1DDb8lQrg130_assertion evidence source_evidence_literature NP518783.RA0qaztfKgkJgW3wtQF679UITSqy4opOWwlb1DDb8lQrg130_provenance.
- NP518783.RA0qaztfKgkJgW3wtQF679UITSqy4opOWwlb1DDb8lQrg130_assertion SIO_000772 20082166 NP518783.RA0qaztfKgkJgW3wtQF679UITSqy4opOWwlb1DDb8lQrg130_provenance.
- NP518783.RA0qaztfKgkJgW3wtQF679UITSqy4opOWwlb1DDb8lQrg130_assertion wasDerivedFrom befree-20150227 NP518783.RA0qaztfKgkJgW3wtQF679UITSqy4opOWwlb1DDb8lQrg130_provenance.
- NP518783.RA0qaztfKgkJgW3wtQF679UITSqy4opOWwlb1DDb8lQrg130_assertion wasGeneratedBy ECO_0000203 NP518783.RA0qaztfKgkJgW3wtQF679UITSqy4opOWwlb1DDb8lQrg130_provenance.
- befree-20150227 importedOn "2015-02-27" NP518783.RA0qaztfKgkJgW3wtQF679UITSqy4opOWwlb1DDb8lQrg130_provenance.