Matches in Nanopublications for { <http://rdf.disgenet.org/nanopublications.trig#NP225881.RAwSIFl_sj_nF1rtytDvoIEiAqcH2hc-3HEMnSEDH0Gxg130_assertion> ?p ?o ?g. }
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- NP225881.RAwSIFl_sj_nF1rtytDvoIEiAqcH2hc-3HEMnSEDH0Gxg130_assertion type Assertion NP225881.RAwSIFl_sj_nF1rtytDvoIEiAqcH2hc-3HEMnSEDH0Gxg130_head.
- NP225881.RAwSIFl_sj_nF1rtytDvoIEiAqcH2hc-3HEMnSEDH0Gxg130_assertion description "[Highly penetrant, non-synonymous, or insertion-deletion mutations in TERF1 and TERF2 were not identified and therefore are not likely to be major genetic risk factors for the development of AA.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP225881.RAwSIFl_sj_nF1rtytDvoIEiAqcH2hc-3HEMnSEDH0Gxg130_provenance.
- NP225881.RAwSIFl_sj_nF1rtytDvoIEiAqcH2hc-3HEMnSEDH0Gxg130_assertion evidence source_evidence_literature NP225881.RAwSIFl_sj_nF1rtytDvoIEiAqcH2hc-3HEMnSEDH0Gxg130_provenance.
- NP225881.RAwSIFl_sj_nF1rtytDvoIEiAqcH2hc-3HEMnSEDH0Gxg130_assertion SIO_000772 16647572 NP225881.RAwSIFl_sj_nF1rtytDvoIEiAqcH2hc-3HEMnSEDH0Gxg130_provenance.
- NP225881.RAwSIFl_sj_nF1rtytDvoIEiAqcH2hc-3HEMnSEDH0Gxg130_assertion wasDerivedFrom befree-20140225 NP225881.RAwSIFl_sj_nF1rtytDvoIEiAqcH2hc-3HEMnSEDH0Gxg130_provenance.
- NP225881.RAwSIFl_sj_nF1rtytDvoIEiAqcH2hc-3HEMnSEDH0Gxg130_assertion wasGeneratedBy ECO_0000203 NP225881.RAwSIFl_sj_nF1rtytDvoIEiAqcH2hc-3HEMnSEDH0Gxg130_provenance.