Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP601098.RAPZZewbdSqGOk7gj8afdV8cr3P8CKCq85TS18xe_fElo130_provenance>. }
Showing items 1 to 9 of
9
with 100 items per page.
- source_evidence_literature type ECO_0000212 NP601098.RAPZZewbdSqGOk7gj8afdV8cr3P8CKCq85TS18xe_fElo130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP601098.RAPZZewbdSqGOk7gj8afdV8cr3P8CKCq85TS18xe_fElo130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP601098.RAPZZewbdSqGOk7gj8afdV8cr3P8CKCq85TS18xe_fElo130_provenance.
- NP601098.RAPZZewbdSqGOk7gj8afdV8cr3P8CKCq85TS18xe_fElo130_assertion description "[A novel mutation in MIP associated with congenital nuclear cataract in a Chinese family.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP601098.RAPZZewbdSqGOk7gj8afdV8cr3P8CKCq85TS18xe_fElo130_provenance.
- NP601098.RAPZZewbdSqGOk7gj8afdV8cr3P8CKCq85TS18xe_fElo130_assertion evidence source_evidence_literature NP601098.RAPZZewbdSqGOk7gj8afdV8cr3P8CKCq85TS18xe_fElo130_provenance.
- NP601098.RAPZZewbdSqGOk7gj8afdV8cr3P8CKCq85TS18xe_fElo130_assertion SIO_000772 21245956 NP601098.RAPZZewbdSqGOk7gj8afdV8cr3P8CKCq85TS18xe_fElo130_provenance.
- NP601098.RAPZZewbdSqGOk7gj8afdV8cr3P8CKCq85TS18xe_fElo130_assertion wasDerivedFrom befree-20140225 NP601098.RAPZZewbdSqGOk7gj8afdV8cr3P8CKCq85TS18xe_fElo130_provenance.
- NP601098.RAPZZewbdSqGOk7gj8afdV8cr3P8CKCq85TS18xe_fElo130_assertion wasGeneratedBy ECO_0000203 NP601098.RAPZZewbdSqGOk7gj8afdV8cr3P8CKCq85TS18xe_fElo130_provenance.
- befree-20140225 importedOn "2014-02-25" NP601098.RAPZZewbdSqGOk7gj8afdV8cr3P8CKCq85TS18xe_fElo130_provenance.