Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP1002241.RAoKFyhWbmglEkFv7vBqEiM0etk3LSYJ2fSH4-6IxTq1Y130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP1002241.RAoKFyhWbmglEkFv7vBqEiM0etk3LSYJ2fSH4-6IxTq1Y130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP1002241.RAoKFyhWbmglEkFv7vBqEiM0etk3LSYJ2fSH4-6IxTq1Y130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP1002241.RAoKFyhWbmglEkFv7vBqEiM0etk3LSYJ2fSH4-6IxTq1Y130_provenance.
- befree-2016 importedOn "2016-02-19" NP1002241.RAoKFyhWbmglEkFv7vBqEiM0etk3LSYJ2fSH4-6IxTq1Y130_provenance.
- NP1002241.RAoKFyhWbmglEkFv7vBqEiM0etk3LSYJ2fSH4-6IxTq1Y130_assertion wasGeneratedBy ECO_0000203 NP1002241.RAoKFyhWbmglEkFv7vBqEiM0etk3LSYJ2fSH4-6IxTq1Y130_provenance.
- NP1002241.RAoKFyhWbmglEkFv7vBqEiM0etk3LSYJ2fSH4-6IxTq1Y130_assertion wasDerivedFrom befree-2016 NP1002241.RAoKFyhWbmglEkFv7vBqEiM0etk3LSYJ2fSH4-6IxTq1Y130_provenance.
- NP1002241.RAoKFyhWbmglEkFv7vBqEiM0etk3LSYJ2fSH4-6IxTq1Y130_assertion SIO_000772 22855342 NP1002241.RAoKFyhWbmglEkFv7vBqEiM0etk3LSYJ2fSH4-6IxTq1Y130_provenance.
- NP1002241.RAoKFyhWbmglEkFv7vBqEiM0etk3LSYJ2fSH4-6IxTq1Y130_assertion evidence source_evidence_literature NP1002241.RAoKFyhWbmglEkFv7vBqEiM0etk3LSYJ2fSH4-6IxTq1Y130_provenance.
- NP1002241.RAoKFyhWbmglEkFv7vBqEiM0etk3LSYJ2fSH4-6IxTq1Y130_assertion description "[Genetic abnormalities, such as those of multiple endocrine neoplasia type 1 (MEN1) and Cyclin D1 (CCND1) genes, occur in <50% of nonhereditary (sporadic) parathyroid adenomas.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1002241.RAoKFyhWbmglEkFv7vBqEiM0etk3LSYJ2fSH4-6IxTq1Y130_provenance.