Matches in Nanopublications for { <http://rdf.disgenet.org/nanopublications.trig#NP404802.RA8P_QBDJmiK2_yxXDqVFVwa_NwdKBzALiUDe5wiaWS6I130_assertion> ?p ?o ?g. }
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- NP404802.RA8P_QBDJmiK2_yxXDqVFVwa_NwdKBzALiUDe5wiaWS6I130_assertion type Assertion NP404802.RA8P_QBDJmiK2_yxXDqVFVwa_NwdKBzALiUDe5wiaWS6I130_head.
- 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.