Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP676274.RAutG3Vb2S2PvHELx_nU2k5qldiw3QETbX_rMaQdG5psc130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP676274.RAutG3Vb2S2PvHELx_nU2k5qldiw3QETbX_rMaQdG5psc130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP676274.RAutG3Vb2S2PvHELx_nU2k5qldiw3QETbX_rMaQdG5psc130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP676274.RAutG3Vb2S2PvHELx_nU2k5qldiw3QETbX_rMaQdG5psc130_provenance.
- NP676274.RAutG3Vb2S2PvHELx_nU2k5qldiw3QETbX_rMaQdG5psc130_assertion description "[We did not observe strong evidence for any of 74 selected POF candidate genes or linkage regions being associated with idiopathic POF in Caucasian females, although suggestive association (P < 0.005) was observed for SNPs that mapped in BDNF, CXCL12, LHR, USP9X and TAF4B.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP676274.RAutG3Vb2S2PvHELx_nU2k5qldiw3QETbX_rMaQdG5psc130_provenance.
- NP676274.RAutG3Vb2S2PvHELx_nU2k5qldiw3QETbX_rMaQdG5psc130_assertion evidence source_evidence_literature NP676274.RAutG3Vb2S2PvHELx_nU2k5qldiw3QETbX_rMaQdG5psc130_provenance.
- NP676274.RAutG3Vb2S2PvHELx_nU2k5qldiw3QETbX_rMaQdG5psc130_assertion SIO_000772 19508998 NP676274.RAutG3Vb2S2PvHELx_nU2k5qldiw3QETbX_rMaQdG5psc130_provenance.
- NP676274.RAutG3Vb2S2PvHELx_nU2k5qldiw3QETbX_rMaQdG5psc130_assertion wasDerivedFrom befree-20140225 NP676274.RAutG3Vb2S2PvHELx_nU2k5qldiw3QETbX_rMaQdG5psc130_provenance.
- NP676274.RAutG3Vb2S2PvHELx_nU2k5qldiw3QETbX_rMaQdG5psc130_assertion wasGeneratedBy ECO_0000203 NP676274.RAutG3Vb2S2PvHELx_nU2k5qldiw3QETbX_rMaQdG5psc130_provenance.
- befree-20140225 importedOn "2014-02-25" NP676274.RAutG3Vb2S2PvHELx_nU2k5qldiw3QETbX_rMaQdG5psc130_provenance.