Matches in Nanopublications for { <http://rdf.disgenet.org/nanopublications.trig#NP697042.RAhq7PXlfYZC_EVpo-f2TLSkDZTcoX-3F290m7OM6-B-o130_assertion> ?p ?o ?g. }
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- NP697042.RAhq7PXlfYZC_EVpo-f2TLSkDZTcoX-3F290m7OM6-B-o130_assertion type Assertion NP697042.RAhq7PXlfYZC_EVpo-f2TLSkDZTcoX-3F290m7OM6-B-o130_head.
- NP697042.RAhq7PXlfYZC_EVpo-f2TLSkDZTcoX-3F290m7OM6-B-o130_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." NP697042.RAhq7PXlfYZC_EVpo-f2TLSkDZTcoX-3F290m7OM6-B-o130_provenance.
- NP697042.RAhq7PXlfYZC_EVpo-f2TLSkDZTcoX-3F290m7OM6-B-o130_assertion evidence source_evidence_literature NP697042.RAhq7PXlfYZC_EVpo-f2TLSkDZTcoX-3F290m7OM6-B-o130_provenance.
- NP697042.RAhq7PXlfYZC_EVpo-f2TLSkDZTcoX-3F290m7OM6-B-o130_assertion SIO_000772 16979636 NP697042.RAhq7PXlfYZC_EVpo-f2TLSkDZTcoX-3F290m7OM6-B-o130_provenance.
- NP697042.RAhq7PXlfYZC_EVpo-f2TLSkDZTcoX-3F290m7OM6-B-o130_assertion wasDerivedFrom befree-20140225 NP697042.RAhq7PXlfYZC_EVpo-f2TLSkDZTcoX-3F290m7OM6-B-o130_provenance.
- NP697042.RAhq7PXlfYZC_EVpo-f2TLSkDZTcoX-3F290m7OM6-B-o130_assertion wasGeneratedBy ECO_0000203 NP697042.RAhq7PXlfYZC_EVpo-f2TLSkDZTcoX-3F290m7OM6-B-o130_provenance.