Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP734849.RAxIcnhQ6bFtrgpe-JuF8KCP8GeuN20ZLAnFy_UwFF8uI130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP734849.RAxIcnhQ6bFtrgpe-JuF8KCP8GeuN20ZLAnFy_UwFF8uI130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP734849.RAxIcnhQ6bFtrgpe-JuF8KCP8GeuN20ZLAnFy_UwFF8uI130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP734849.RAxIcnhQ6bFtrgpe-JuF8KCP8GeuN20ZLAnFy_UwFF8uI130_provenance.
- NP734849.RAxIcnhQ6bFtrgpe-JuF8KCP8GeuN20ZLAnFy_UwFF8uI130_assertion description "[Potentially causal mutations in FOXO3A (2/90; 2.2%) and FOXO1A (1/90; 1.1%) were identified in POF patients; however, the pathological role of these mutations will be determined only by screening increased numbers of patients and controls, or by functional studies.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP734849.RAxIcnhQ6bFtrgpe-JuF8KCP8GeuN20ZLAnFy_UwFF8uI130_provenance.
- NP734849.RAxIcnhQ6bFtrgpe-JuF8KCP8GeuN20ZLAnFy_UwFF8uI130_assertion evidence source_evidence_literature NP734849.RAxIcnhQ6bFtrgpe-JuF8KCP8GeuN20ZLAnFy_UwFF8uI130_provenance.
- NP734849.RAxIcnhQ6bFtrgpe-JuF8KCP8GeuN20ZLAnFy_UwFF8uI130_assertion SIO_000772 16979636 NP734849.RAxIcnhQ6bFtrgpe-JuF8KCP8GeuN20ZLAnFy_UwFF8uI130_provenance.
- NP734849.RAxIcnhQ6bFtrgpe-JuF8KCP8GeuN20ZLAnFy_UwFF8uI130_assertion wasDerivedFrom befree-20140225 NP734849.RAxIcnhQ6bFtrgpe-JuF8KCP8GeuN20ZLAnFy_UwFF8uI130_provenance.
- NP734849.RAxIcnhQ6bFtrgpe-JuF8KCP8GeuN20ZLAnFy_UwFF8uI130_assertion wasGeneratedBy ECO_0000203 NP734849.RAxIcnhQ6bFtrgpe-JuF8KCP8GeuN20ZLAnFy_UwFF8uI130_provenance.
- befree-20140225 importedOn "2014-02-25" NP734849.RAxIcnhQ6bFtrgpe-JuF8KCP8GeuN20ZLAnFy_UwFF8uI130_provenance.