Matches in Nanopublications for { <http://rdf.disgenet.org/nanopublications.trig#NP482835.RAZ3DADUOLVaDLnsoOViAis3445AenDmKnRDuJuGSRn_w130_assertion> ?p ?o ?g. }
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- NP482835.RAZ3DADUOLVaDLnsoOViAis3445AenDmKnRDuJuGSRn_w130_assertion type Assertion NP482835.RAZ3DADUOLVaDLnsoOViAis3445AenDmKnRDuJuGSRn_w130_head.
- NP482835.RAZ3DADUOLVaDLnsoOViAis3445AenDmKnRDuJuGSRn_w130_assertion description "[Cubilin P1297L mutation associated with hereditary megaloblastic anemia 1 causes impaired recognition of intrinsic factor-vitamin B(12) by cubilin.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP482835.RAZ3DADUOLVaDLnsoOViAis3445AenDmKnRDuJuGSRn_w130_provenance.
- NP482835.RAZ3DADUOLVaDLnsoOViAis3445AenDmKnRDuJuGSRn_w130_assertion evidence source_evidence_literature NP482835.RAZ3DADUOLVaDLnsoOViAis3445AenDmKnRDuJuGSRn_w130_provenance.
- NP482835.RAZ3DADUOLVaDLnsoOViAis3445AenDmKnRDuJuGSRn_w130_assertion SIO_000772 10887099 NP482835.RAZ3DADUOLVaDLnsoOViAis3445AenDmKnRDuJuGSRn_w130_provenance.
- NP482835.RAZ3DADUOLVaDLnsoOViAis3445AenDmKnRDuJuGSRn_w130_assertion wasDerivedFrom befree-20140225 NP482835.RAZ3DADUOLVaDLnsoOViAis3445AenDmKnRDuJuGSRn_w130_provenance.
- NP482835.RAZ3DADUOLVaDLnsoOViAis3445AenDmKnRDuJuGSRn_w130_assertion wasGeneratedBy ECO_0000203 NP482835.RAZ3DADUOLVaDLnsoOViAis3445AenDmKnRDuJuGSRn_w130_provenance.