Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP916525.RAgx2hd9ORdiCrGhgE_P8bj2_O3qhjaYs5GAZ8TI3AoK0130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP916525.RAgx2hd9ORdiCrGhgE_P8bj2_O3qhjaYs5GAZ8TI3AoK0130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP916525.RAgx2hd9ORdiCrGhgE_P8bj2_O3qhjaYs5GAZ8TI3AoK0130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP916525.RAgx2hd9ORdiCrGhgE_P8bj2_O3qhjaYs5GAZ8TI3AoK0130_provenance.
- NP916525.RAgx2hd9ORdiCrGhgE_P8bj2_O3qhjaYs5GAZ8TI3AoK0130_assertion description "[Identification and characterization of mutations in FANCL gene: a second case of Fanconi anemia belonging to FA-L complementation group.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP916525.RAgx2hd9ORdiCrGhgE_P8bj2_O3qhjaYs5GAZ8TI3AoK0130_provenance.
- NP916525.RAgx2hd9ORdiCrGhgE_P8bj2_O3qhjaYs5GAZ8TI3AoK0130_assertion evidence source_evidence_literature NP916525.RAgx2hd9ORdiCrGhgE_P8bj2_O3qhjaYs5GAZ8TI3AoK0130_provenance.
- NP916525.RAgx2hd9ORdiCrGhgE_P8bj2_O3qhjaYs5GAZ8TI3AoK0130_assertion SIO_000772 19405097 NP916525.RAgx2hd9ORdiCrGhgE_P8bj2_O3qhjaYs5GAZ8TI3AoK0130_provenance.
- NP916525.RAgx2hd9ORdiCrGhgE_P8bj2_O3qhjaYs5GAZ8TI3AoK0130_assertion wasDerivedFrom befree-20150227 NP916525.RAgx2hd9ORdiCrGhgE_P8bj2_O3qhjaYs5GAZ8TI3AoK0130_provenance.
- NP916525.RAgx2hd9ORdiCrGhgE_P8bj2_O3qhjaYs5GAZ8TI3AoK0130_assertion wasGeneratedBy ECO_0000203 NP916525.RAgx2hd9ORdiCrGhgE_P8bj2_O3qhjaYs5GAZ8TI3AoK0130_provenance.
- befree-20150227 importedOn "2015-02-27" NP916525.RAgx2hd9ORdiCrGhgE_P8bj2_O3qhjaYs5GAZ8TI3AoK0130_provenance.