Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP13454.RA1pE_RGqrMwJsLWVKSKzg7GKHlJY0Vyu4v1V1gMEd5Sw130_provenance>. }
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- source_evidence_curated type ECO_0000205 NP13454.RA1pE_RGqrMwJsLWVKSKzg7GKHlJY0Vyu4v1V1gMEd5Sw130_provenance.
- source_evidence_curated label "DisGeNET evidence - CURATED" NP13454.RA1pE_RGqrMwJsLWVKSKzg7GKHlJY0Vyu4v1V1gMEd5Sw130_provenance.
- source_evidence_curated comment "Gene-disease associations manually curated." NP13454.RA1pE_RGqrMwJsLWVKSKzg7GKHlJY0Vyu4v1V1gMEd5Sw130_provenance.
- NP13454.RA1pE_RGqrMwJsLWVKSKzg7GKHlJY0Vyu4v1V1gMEd5Sw130_assertion description "[The present study investigated CYP2C9 in regard to its allelic variants in 23 tumor samples (10 breast tumors, 1 breast tumor cell line, 5 brain tumors, 7 glioma cell lines) with restriction fragment length polymorphism polymerase chain reaction (RFLP-PCR).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP13454.RA1pE_RGqrMwJsLWVKSKzg7GKHlJY0Vyu4v1V1gMEd5Sw130_provenance.
- NP13454.RA1pE_RGqrMwJsLWVKSKzg7GKHlJY0Vyu4v1V1gMEd5Sw130_assertion evidence source_evidence_curated NP13454.RA1pE_RGqrMwJsLWVKSKzg7GKHlJY0Vyu4v1V1gMEd5Sw130_provenance.
- NP13454.RA1pE_RGqrMwJsLWVKSKzg7GKHlJY0Vyu4v1V1gMEd5Sw130_assertion SIO_000772 16475710 NP13454.RA1pE_RGqrMwJsLWVKSKzg7GKHlJY0Vyu4v1V1gMEd5Sw130_provenance.
- NP13454.RA1pE_RGqrMwJsLWVKSKzg7GKHlJY0Vyu4v1V1gMEd5Sw130_assertion wasDerivedFrom ctd_human-20130708 NP13454.RA1pE_RGqrMwJsLWVKSKzg7GKHlJY0Vyu4v1V1gMEd5Sw130_provenance.
- NP13454.RA1pE_RGqrMwJsLWVKSKzg7GKHlJY0Vyu4v1V1gMEd5Sw130_assertion wasGeneratedBy ECO_0000218 NP13454.RA1pE_RGqrMwJsLWVKSKzg7GKHlJY0Vyu4v1V1gMEd5Sw130_provenance.
- ctd_human-20130708 importedOn "2013-07-24" NP13454.RA1pE_RGqrMwJsLWVKSKzg7GKHlJY0Vyu4v1V1gMEd5Sw130_provenance.