Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP521177.RA6KWaM9Q7o33dHmNTSvO8a_RvQmGRU8F0vxo_gSjgxqI130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP521177.RA6KWaM9Q7o33dHmNTSvO8a_RvQmGRU8F0vxo_gSjgxqI130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP521177.RA6KWaM9Q7o33dHmNTSvO8a_RvQmGRU8F0vxo_gSjgxqI130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP521177.RA6KWaM9Q7o33dHmNTSvO8a_RvQmGRU8F0vxo_gSjgxqI130_provenance.
- befree-2016 importedOn "2016-02-19" NP521177.RA6KWaM9Q7o33dHmNTSvO8a_RvQmGRU8F0vxo_gSjgxqI130_provenance.
- NP521177.RA6KWaM9Q7o33dHmNTSvO8a_RvQmGRU8F0vxo_gSjgxqI130_assertion wasGeneratedBy ECO_0000203 NP521177.RA6KWaM9Q7o33dHmNTSvO8a_RvQmGRU8F0vxo_gSjgxqI130_provenance.
- NP521177.RA6KWaM9Q7o33dHmNTSvO8a_RvQmGRU8F0vxo_gSjgxqI130_assertion wasDerivedFrom befree-2016 NP521177.RA6KWaM9Q7o33dHmNTSvO8a_RvQmGRU8F0vxo_gSjgxqI130_provenance.
- NP521177.RA6KWaM9Q7o33dHmNTSvO8a_RvQmGRU8F0vxo_gSjgxqI130_assertion SIO_000772 16272056 NP521177.RA6KWaM9Q7o33dHmNTSvO8a_RvQmGRU8F0vxo_gSjgxqI130_provenance.
- NP521177.RA6KWaM9Q7o33dHmNTSvO8a_RvQmGRU8F0vxo_gSjgxqI130_assertion evidence source_evidence_literature NP521177.RA6KWaM9Q7o33dHmNTSvO8a_RvQmGRU8F0vxo_gSjgxqI130_provenance.
- NP521177.RA6KWaM9Q7o33dHmNTSvO8a_RvQmGRU8F0vxo_gSjgxqI130_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." NP521177.RA6KWaM9Q7o33dHmNTSvO8a_RvQmGRU8F0vxo_gSjgxqI130_provenance.