Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP404802.RA8P_QBDJmiK2_yxXDqVFVwa_NwdKBzALiUDe5wiaWS6I130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP404802.RA8P_QBDJmiK2_yxXDqVFVwa_NwdKBzALiUDe5wiaWS6I130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP404802.RA8P_QBDJmiK2_yxXDqVFVwa_NwdKBzALiUDe5wiaWS6I130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP404802.RA8P_QBDJmiK2_yxXDqVFVwa_NwdKBzALiUDe5wiaWS6I130_provenance.
- NP404802.RA8P_QBDJmiK2_yxXDqVFVwa_NwdKBzALiUDe5wiaWS6I130_assertion wasGeneratedBy ECO_0000203 NP404802.RA8P_QBDJmiK2_yxXDqVFVwa_NwdKBzALiUDe5wiaWS6I130_provenance.
- NP404802.RA8P_QBDJmiK2_yxXDqVFVwa_NwdKBzALiUDe5wiaWS6I130_assertion wasDerivedFrom befree-20140225 NP404802.RA8P_QBDJmiK2_yxXDqVFVwa_NwdKBzALiUDe5wiaWS6I130_provenance.
- NP404802.RA8P_QBDJmiK2_yxXDqVFVwa_NwdKBzALiUDe5wiaWS6I130_assertion SIO_000772 23434763 NP404802.RA8P_QBDJmiK2_yxXDqVFVwa_NwdKBzALiUDe5wiaWS6I130_provenance.
- NP404802.RA8P_QBDJmiK2_yxXDqVFVwa_NwdKBzALiUDe5wiaWS6I130_assertion evidence source_evidence_literature NP404802.RA8P_QBDJmiK2_yxXDqVFVwa_NwdKBzALiUDe5wiaWS6I130_provenance.
- NP404802.RA8P_QBDJmiK2_yxXDqVFVwa_NwdKBzALiUDe5wiaWS6I130_assertion description "[Recessive inactivating mutations in WNT1 are a new cause of OI type IV.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP404802.RA8P_QBDJmiK2_yxXDqVFVwa_NwdKBzALiUDe5wiaWS6I130_provenance.
- befree-20140225 importedOn "2014-02-25" NP404802.RA8P_QBDJmiK2_yxXDqVFVwa_NwdKBzALiUDe5wiaWS6I130_provenance.