Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP1401616.RArnVrEXV6L_rWbBSbDn2ZfckhwbsBPdxqWDV1ySBl0F8130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP1401616.RArnVrEXV6L_rWbBSbDn2ZfckhwbsBPdxqWDV1ySBl0F8130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP1401616.RArnVrEXV6L_rWbBSbDn2ZfckhwbsBPdxqWDV1ySBl0F8130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP1401616.RArnVrEXV6L_rWbBSbDn2ZfckhwbsBPdxqWDV1ySBl0F8130_provenance.
- NP1401616.RArnVrEXV6L_rWbBSbDn2ZfckhwbsBPdxqWDV1ySBl0F8130_assertion description "[Mutations in the Delta1-pyrroline 5-carboxylate dehydrogenase gene cause type II hyperprolinemia.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1401616.RArnVrEXV6L_rWbBSbDn2ZfckhwbsBPdxqWDV1ySBl0F8130_provenance.
- NP1401616.RArnVrEXV6L_rWbBSbDn2ZfckhwbsBPdxqWDV1ySBl0F8130_assertion evidence source_evidence_literature NP1401616.RArnVrEXV6L_rWbBSbDn2ZfckhwbsBPdxqWDV1ySBl0F8130_provenance.
- NP1401616.RArnVrEXV6L_rWbBSbDn2ZfckhwbsBPdxqWDV1ySBl0F8130_assertion SIO_000772 9700195 NP1401616.RArnVrEXV6L_rWbBSbDn2ZfckhwbsBPdxqWDV1ySBl0F8130_provenance.
- NP1401616.RArnVrEXV6L_rWbBSbDn2ZfckhwbsBPdxqWDV1ySBl0F8130_assertion wasDerivedFrom befree-2016 NP1401616.RArnVrEXV6L_rWbBSbDn2ZfckhwbsBPdxqWDV1ySBl0F8130_provenance.
- NP1401616.RArnVrEXV6L_rWbBSbDn2ZfckhwbsBPdxqWDV1ySBl0F8130_assertion wasGeneratedBy ECO_0000203 NP1401616.RArnVrEXV6L_rWbBSbDn2ZfckhwbsBPdxqWDV1ySBl0F8130_provenance.
- befree-2016 importedOn "2016-02-19" NP1401616.RArnVrEXV6L_rWbBSbDn2ZfckhwbsBPdxqWDV1ySBl0F8130_provenance.