Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP973676.RANtU0a429v-okJquvsNcwTZQkT1XsdXa7ssXwPnCEpE4130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP973676.RANtU0a429v-okJquvsNcwTZQkT1XsdXa7ssXwPnCEpE4130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP973676.RANtU0a429v-okJquvsNcwTZQkT1XsdXa7ssXwPnCEpE4130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP973676.RANtU0a429v-okJquvsNcwTZQkT1XsdXa7ssXwPnCEpE4130_provenance.
- befree-2016 importedOn "2016-02-19" NP973676.RANtU0a429v-okJquvsNcwTZQkT1XsdXa7ssXwPnCEpE4130_provenance.
- NP973676.RANtU0a429v-okJquvsNcwTZQkT1XsdXa7ssXwPnCEpE4130_assertion wasGeneratedBy ECO_0000203 NP973676.RANtU0a429v-okJquvsNcwTZQkT1XsdXa7ssXwPnCEpE4130_provenance.
- NP973676.RANtU0a429v-okJquvsNcwTZQkT1XsdXa7ssXwPnCEpE4130_assertion wasDerivedFrom befree-2016 NP973676.RANtU0a429v-okJquvsNcwTZQkT1XsdXa7ssXwPnCEpE4130_provenance.
- NP973676.RANtU0a429v-okJquvsNcwTZQkT1XsdXa7ssXwPnCEpE4130_assertion SIO_000772 22490426 NP973676.RANtU0a429v-okJquvsNcwTZQkT1XsdXa7ssXwPnCEpE4130_provenance.
- NP973676.RANtU0a429v-okJquvsNcwTZQkT1XsdXa7ssXwPnCEpE4130_assertion evidence source_evidence_literature NP973676.RANtU0a429v-okJquvsNcwTZQkT1XsdXa7ssXwPnCEpE4130_provenance.
- NP973676.RANtU0a429v-okJquvsNcwTZQkT1XsdXa7ssXwPnCEpE4130_assertion description "[Pelizaeus-Merzbacher disease (PMD; MIM#312080) is a rare X-linked leukodystrophy presenting with motor developmental delay associated with spasticity and nystagmus.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP973676.RANtU0a429v-okJquvsNcwTZQkT1XsdXa7ssXwPnCEpE4130_provenance.