Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP232324.RASiL5HDiV-kRSGSVnpR-wT6pxJGkqsCQIOX9m_d9hSwg130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP232324.RASiL5HDiV-kRSGSVnpR-wT6pxJGkqsCQIOX9m_d9hSwg130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP232324.RASiL5HDiV-kRSGSVnpR-wT6pxJGkqsCQIOX9m_d9hSwg130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP232324.RASiL5HDiV-kRSGSVnpR-wT6pxJGkqsCQIOX9m_d9hSwg130_provenance.
- NP232324.RASiL5HDiV-kRSGSVnpR-wT6pxJGkqsCQIOX9m_d9hSwg130_assertion description "[Familial isolated primary hyperparathyroidism is a distinct genetic variant of the MEN1 syndrome.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP232324.RASiL5HDiV-kRSGSVnpR-wT6pxJGkqsCQIOX9m_d9hSwg130_provenance.
- NP232324.RASiL5HDiV-kRSGSVnpR-wT6pxJGkqsCQIOX9m_d9hSwg130_assertion evidence source_evidence_literature NP232324.RASiL5HDiV-kRSGSVnpR-wT6pxJGkqsCQIOX9m_d9hSwg130_provenance.
- NP232324.RASiL5HDiV-kRSGSVnpR-wT6pxJGkqsCQIOX9m_d9hSwg130_assertion SIO_000772 18084346 NP232324.RASiL5HDiV-kRSGSVnpR-wT6pxJGkqsCQIOX9m_d9hSwg130_provenance.
- NP232324.RASiL5HDiV-kRSGSVnpR-wT6pxJGkqsCQIOX9m_d9hSwg130_assertion wasDerivedFrom lhgdn-20090331 NP232324.RASiL5HDiV-kRSGSVnpR-wT6pxJGkqsCQIOX9m_d9hSwg130_provenance.
- NP232324.RASiL5HDiV-kRSGSVnpR-wT6pxJGkqsCQIOX9m_d9hSwg130_assertion wasGeneratedBy ECO_0000203 NP232324.RASiL5HDiV-kRSGSVnpR-wT6pxJGkqsCQIOX9m_d9hSwg130_provenance.
- lhgdn-20090331 importedOn "2009-03-31" NP232324.RASiL5HDiV-kRSGSVnpR-wT6pxJGkqsCQIOX9m_d9hSwg130_provenance.