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- source_evidence_literature type ECO_0000212 NP452942.RACIpVhxXp7wYwq9zTfilU3GKJH4bL_TKWOD9KnM_VlK0130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP452942.RACIpVhxXp7wYwq9zTfilU3GKJH4bL_TKWOD9KnM_VlK0130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP452942.RACIpVhxXp7wYwq9zTfilU3GKJH4bL_TKWOD9KnM_VlK0130_provenance.
- NP452942.RACIpVhxXp7wYwq9zTfilU3GKJH4bL_TKWOD9KnM_VlK0130_assertion description "[Identification of a common PEX1 mutation in Zellweger syndrome.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP452942.RACIpVhxXp7wYwq9zTfilU3GKJH4bL_TKWOD9KnM_VlK0130_provenance.
- NP452942.RACIpVhxXp7wYwq9zTfilU3GKJH4bL_TKWOD9KnM_VlK0130_assertion evidence source_evidence_literature NP452942.RACIpVhxXp7wYwq9zTfilU3GKJH4bL_TKWOD9KnM_VlK0130_provenance.
- NP452942.RACIpVhxXp7wYwq9zTfilU3GKJH4bL_TKWOD9KnM_VlK0130_assertion SIO_000772 10447258 NP452942.RACIpVhxXp7wYwq9zTfilU3GKJH4bL_TKWOD9KnM_VlK0130_provenance.
- NP452942.RACIpVhxXp7wYwq9zTfilU3GKJH4bL_TKWOD9KnM_VlK0130_assertion wasDerivedFrom befree-20140225 NP452942.RACIpVhxXp7wYwq9zTfilU3GKJH4bL_TKWOD9KnM_VlK0130_provenance.
- NP452942.RACIpVhxXp7wYwq9zTfilU3GKJH4bL_TKWOD9KnM_VlK0130_assertion wasGeneratedBy ECO_0000203 NP452942.RACIpVhxXp7wYwq9zTfilU3GKJH4bL_TKWOD9KnM_VlK0130_provenance.
- befree-20140225 importedOn "2014-02-25" NP452942.RACIpVhxXp7wYwq9zTfilU3GKJH4bL_TKWOD9KnM_VlK0130_provenance.