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- source_evidence_literature type ECO_0000212 NP1009196.RAsVbINB98Pgal9BqUp97Su1lIalX9T3IxMstjBgw5djU130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP1009196.RAsVbINB98Pgal9BqUp97Su1lIalX9T3IxMstjBgw5djU130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP1009196.RAsVbINB98Pgal9BqUp97Su1lIalX9T3IxMstjBgw5djU130_provenance.
- befree-20150227 importedOn "2015-02-27" NP1009196.RAsVbINB98Pgal9BqUp97Su1lIalX9T3IxMstjBgw5djU130_provenance.
- NP1009196.RAsVbINB98Pgal9BqUp97Su1lIalX9T3IxMstjBgw5djU130_assertion wasGeneratedBy ECO_0000203 NP1009196.RAsVbINB98Pgal9BqUp97Su1lIalX9T3IxMstjBgw5djU130_provenance.
- NP1009196.RAsVbINB98Pgal9BqUp97Su1lIalX9T3IxMstjBgw5djU130_assertion wasDerivedFrom befree-20150227 NP1009196.RAsVbINB98Pgal9BqUp97Su1lIalX9T3IxMstjBgw5djU130_provenance.
- NP1009196.RAsVbINB98Pgal9BqUp97Su1lIalX9T3IxMstjBgw5djU130_assertion SIO_000772 16272056 NP1009196.RAsVbINB98Pgal9BqUp97Su1lIalX9T3IxMstjBgw5djU130_provenance.
- NP1009196.RAsVbINB98Pgal9BqUp97Su1lIalX9T3IxMstjBgw5djU130_assertion evidence source_evidence_literature NP1009196.RAsVbINB98Pgal9BqUp97Su1lIalX9T3IxMstjBgw5djU130_provenance.
- NP1009196.RAsVbINB98Pgal9BqUp97Su1lIalX9T3IxMstjBgw5djU130_assertion description "[Mutations in the inosine monophosphate dehydrogenase 1 gene (IMPDH1) have recently been discovered to cause a form of autosomal dominant retinitis pigmentosa (adRP).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1009196.RAsVbINB98Pgal9BqUp97Su1lIalX9T3IxMstjBgw5djU130_provenance.