Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP492475.RAPs6NSnIMm8BTLMZuDg3a8_IoqfNp7wWaDiJRUu7QhbA130_provenance>. }
Showing items 1 to 9 of
9
with 100 items per page.
- source_evidence_literature type ECO_0000212 NP492475.RAPs6NSnIMm8BTLMZuDg3a8_IoqfNp7wWaDiJRUu7QhbA130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP492475.RAPs6NSnIMm8BTLMZuDg3a8_IoqfNp7wWaDiJRUu7QhbA130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP492475.RAPs6NSnIMm8BTLMZuDg3a8_IoqfNp7wWaDiJRUu7QhbA130_provenance.
- NP492475.RAPs6NSnIMm8BTLMZuDg3a8_IoqfNp7wWaDiJRUu7QhbA130_assertion description "[A novel COL1A1 mutation in infantile cortical hyperostosis (Caffey disease) expands the spectrum of collagen-related disorders.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP492475.RAPs6NSnIMm8BTLMZuDg3a8_IoqfNp7wWaDiJRUu7QhbA130_provenance.
- NP492475.RAPs6NSnIMm8BTLMZuDg3a8_IoqfNp7wWaDiJRUu7QhbA130_assertion evidence source_evidence_literature NP492475.RAPs6NSnIMm8BTLMZuDg3a8_IoqfNp7wWaDiJRUu7QhbA130_provenance.
- NP492475.RAPs6NSnIMm8BTLMZuDg3a8_IoqfNp7wWaDiJRUu7QhbA130_assertion SIO_000772 15864348 NP492475.RAPs6NSnIMm8BTLMZuDg3a8_IoqfNp7wWaDiJRUu7QhbA130_provenance.
- NP492475.RAPs6NSnIMm8BTLMZuDg3a8_IoqfNp7wWaDiJRUu7QhbA130_assertion wasDerivedFrom befree-2016 NP492475.RAPs6NSnIMm8BTLMZuDg3a8_IoqfNp7wWaDiJRUu7QhbA130_provenance.
- NP492475.RAPs6NSnIMm8BTLMZuDg3a8_IoqfNp7wWaDiJRUu7QhbA130_assertion wasGeneratedBy ECO_0000203 NP492475.RAPs6NSnIMm8BTLMZuDg3a8_IoqfNp7wWaDiJRUu7QhbA130_provenance.
- befree-2016 importedOn "2016-02-19" NP492475.RAPs6NSnIMm8BTLMZuDg3a8_IoqfNp7wWaDiJRUu7QhbA130_provenance.