Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP225881.RAwSIFl_sj_nF1rtytDvoIEiAqcH2hc-3HEMnSEDH0Gxg130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP225881.RAwSIFl_sj_nF1rtytDvoIEiAqcH2hc-3HEMnSEDH0Gxg130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP225881.RAwSIFl_sj_nF1rtytDvoIEiAqcH2hc-3HEMnSEDH0Gxg130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP225881.RAwSIFl_sj_nF1rtytDvoIEiAqcH2hc-3HEMnSEDH0Gxg130_provenance.
- 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.
- befree-20140225 importedOn "2014-02-25" NP225881.RAwSIFl_sj_nF1rtytDvoIEiAqcH2hc-3HEMnSEDH0Gxg130_provenance.