Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP868861.RAFpLehrb0PuhX7Vjm0SJivwTZBtSY5eTeR_VL5n6f3NY130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP868861.RAFpLehrb0PuhX7Vjm0SJivwTZBtSY5eTeR_VL5n6f3NY130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP868861.RAFpLehrb0PuhX7Vjm0SJivwTZBtSY5eTeR_VL5n6f3NY130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP868861.RAFpLehrb0PuhX7Vjm0SJivwTZBtSY5eTeR_VL5n6f3NY130_provenance.
- NP868861.RAFpLehrb0PuhX7Vjm0SJivwTZBtSY5eTeR_VL5n6f3NY130_assertion description "[Other features noted in this kindred including epilepsy, cognitive impairment, depression, and migraine did not segregate with the HSP phenotype or mutation, and therefore the significance of these features to SPG4 is unclear.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP868861.RAFpLehrb0PuhX7Vjm0SJivwTZBtSY5eTeR_VL5n6f3NY130_provenance.
- NP868861.RAFpLehrb0PuhX7Vjm0SJivwTZBtSY5eTeR_VL5n6f3NY130_assertion evidence source_evidence_literature NP868861.RAFpLehrb0PuhX7Vjm0SJivwTZBtSY5eTeR_VL5n6f3NY130_provenance.
- NP868861.RAFpLehrb0PuhX7Vjm0SJivwTZBtSY5eTeR_VL5n6f3NY130_assertion SIO_000772 15667412 NP868861.RAFpLehrb0PuhX7Vjm0SJivwTZBtSY5eTeR_VL5n6f3NY130_provenance.
- NP868861.RAFpLehrb0PuhX7Vjm0SJivwTZBtSY5eTeR_VL5n6f3NY130_assertion wasDerivedFrom befree-20140225 NP868861.RAFpLehrb0PuhX7Vjm0SJivwTZBtSY5eTeR_VL5n6f3NY130_provenance.
- NP868861.RAFpLehrb0PuhX7Vjm0SJivwTZBtSY5eTeR_VL5n6f3NY130_assertion wasGeneratedBy ECO_0000203 NP868861.RAFpLehrb0PuhX7Vjm0SJivwTZBtSY5eTeR_VL5n6f3NY130_provenance.
- befree-20140225 importedOn "2014-02-25" NP868861.RAFpLehrb0PuhX7Vjm0SJivwTZBtSY5eTeR_VL5n6f3NY130_provenance.