Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP718719.RAk5cj2-1X-gaQ2dwS7Ak9FNp9rqDCRPJhXt9fzLeM9ng130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP718719.RAk5cj2-1X-gaQ2dwS7Ak9FNp9rqDCRPJhXt9fzLeM9ng130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP718719.RAk5cj2-1X-gaQ2dwS7Ak9FNp9rqDCRPJhXt9fzLeM9ng130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP718719.RAk5cj2-1X-gaQ2dwS7Ak9FNp9rqDCRPJhXt9fzLeM9ng130_provenance.
- NP718719.RAk5cj2-1X-gaQ2dwS7Ak9FNp9rqDCRPJhXt9fzLeM9ng130_assertion description "[Expanding the phenotypes of the Pro56Ser VAPB mutation: proximal SMA with dysautonomia.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP718719.RAk5cj2-1X-gaQ2dwS7Ak9FNp9rqDCRPJhXt9fzLeM9ng130_provenance.
- NP718719.RAk5cj2-1X-gaQ2dwS7Ak9FNp9rqDCRPJhXt9fzLeM9ng130_assertion evidence source_evidence_literature NP718719.RAk5cj2-1X-gaQ2dwS7Ak9FNp9rqDCRPJhXt9fzLeM9ng130_provenance.
- NP718719.RAk5cj2-1X-gaQ2dwS7Ak9FNp9rqDCRPJhXt9fzLeM9ng130_assertion SIO_000772 16967488 NP718719.RAk5cj2-1X-gaQ2dwS7Ak9FNp9rqDCRPJhXt9fzLeM9ng130_provenance.
- NP718719.RAk5cj2-1X-gaQ2dwS7Ak9FNp9rqDCRPJhXt9fzLeM9ng130_assertion wasDerivedFrom befree-20140225 NP718719.RAk5cj2-1X-gaQ2dwS7Ak9FNp9rqDCRPJhXt9fzLeM9ng130_provenance.
- NP718719.RAk5cj2-1X-gaQ2dwS7Ak9FNp9rqDCRPJhXt9fzLeM9ng130_assertion wasGeneratedBy ECO_0000203 NP718719.RAk5cj2-1X-gaQ2dwS7Ak9FNp9rqDCRPJhXt9fzLeM9ng130_provenance.
- befree-20140225 importedOn "2014-02-25" NP718719.RAk5cj2-1X-gaQ2dwS7Ak9FNp9rqDCRPJhXt9fzLeM9ng130_provenance.