Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP348198.RAxm-eM05hfgJFeSLfU7kHcO9pBxdjQaJdm2xeBxS1csU130_provenance>. }
Showing items 1 to 9 of
9
with 100 items per page.
- source_evidence_literature type ECO_0000212 NP348198.RAxm-eM05hfgJFeSLfU7kHcO9pBxdjQaJdm2xeBxS1csU130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP348198.RAxm-eM05hfgJFeSLfU7kHcO9pBxdjQaJdm2xeBxS1csU130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP348198.RAxm-eM05hfgJFeSLfU7kHcO9pBxdjQaJdm2xeBxS1csU130_provenance.
- NP348198.RAxm-eM05hfgJFeSLfU7kHcO9pBxdjQaJdm2xeBxS1csU130_assertion description "[Two additional IMPDH1 variants, Arg105Trp and Asn198Lys, were found in two patients with isolated LCA.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP348198.RAxm-eM05hfgJFeSLfU7kHcO9pBxdjQaJdm2xeBxS1csU130_provenance.
- NP348198.RAxm-eM05hfgJFeSLfU7kHcO9pBxdjQaJdm2xeBxS1csU130_assertion evidence source_evidence_literature NP348198.RAxm-eM05hfgJFeSLfU7kHcO9pBxdjQaJdm2xeBxS1csU130_provenance.
- NP348198.RAxm-eM05hfgJFeSLfU7kHcO9pBxdjQaJdm2xeBxS1csU130_assertion SIO_000772 16384941 NP348198.RAxm-eM05hfgJFeSLfU7kHcO9pBxdjQaJdm2xeBxS1csU130_provenance.
- NP348198.RAxm-eM05hfgJFeSLfU7kHcO9pBxdjQaJdm2xeBxS1csU130_assertion wasDerivedFrom befree-20140225 NP348198.RAxm-eM05hfgJFeSLfU7kHcO9pBxdjQaJdm2xeBxS1csU130_provenance.
- NP348198.RAxm-eM05hfgJFeSLfU7kHcO9pBxdjQaJdm2xeBxS1csU130_assertion wasGeneratedBy ECO_0000203 NP348198.RAxm-eM05hfgJFeSLfU7kHcO9pBxdjQaJdm2xeBxS1csU130_provenance.
- befree-20140225 importedOn "2014-02-25" NP348198.RAxm-eM05hfgJFeSLfU7kHcO9pBxdjQaJdm2xeBxS1csU130_provenance.