Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP305839.RAQFT_MJ5AbfM_xbYiV0loARZjVpnBlpFGEQzo3fZWRFc130_provenance>. }
Showing items 1 to 9 of
9
with 100 items per page.
- source_evidence_literature type ECO_0000212 NP305839.RAQFT_MJ5AbfM_xbYiV0loARZjVpnBlpFGEQzo3fZWRFc130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP305839.RAQFT_MJ5AbfM_xbYiV0loARZjVpnBlpFGEQzo3fZWRFc130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP305839.RAQFT_MJ5AbfM_xbYiV0loARZjVpnBlpFGEQzo3fZWRFc130_provenance.
- NP305839.RAQFT_MJ5AbfM_xbYiV0loARZjVpnBlpFGEQzo3fZWRFc130_assertion description "[The data expand the clinical spectrum of TH deficiency and suggest that TH mutations may account for some patients with DRD simulating spastic paraplegia.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP305839.RAQFT_MJ5AbfM_xbYiV0loARZjVpnBlpFGEQzo3fZWRFc130_provenance.
- NP305839.RAQFT_MJ5AbfM_xbYiV0loARZjVpnBlpFGEQzo3fZWRFc130_assertion evidence source_evidence_literature NP305839.RAQFT_MJ5AbfM_xbYiV0loARZjVpnBlpFGEQzo3fZWRFc130_provenance.
- NP305839.RAQFT_MJ5AbfM_xbYiV0loARZjVpnBlpFGEQzo3fZWRFc130_assertion SIO_000772 11160968 NP305839.RAQFT_MJ5AbfM_xbYiV0loARZjVpnBlpFGEQzo3fZWRFc130_provenance.
- NP305839.RAQFT_MJ5AbfM_xbYiV0loARZjVpnBlpFGEQzo3fZWRFc130_assertion wasDerivedFrom befree-2016 NP305839.RAQFT_MJ5AbfM_xbYiV0loARZjVpnBlpFGEQzo3fZWRFc130_provenance.
- NP305839.RAQFT_MJ5AbfM_xbYiV0loARZjVpnBlpFGEQzo3fZWRFc130_assertion wasGeneratedBy ECO_0000203 NP305839.RAQFT_MJ5AbfM_xbYiV0loARZjVpnBlpFGEQzo3fZWRFc130_provenance.
- befree-2016 importedOn "2016-02-19" NP305839.RAQFT_MJ5AbfM_xbYiV0loARZjVpnBlpFGEQzo3fZWRFc130_provenance.