Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP700963.RAVbCUx9_4VxMr_GdkC2CiE7OvN6Mh1VmZFNYOECRUYQo130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP700963.RAVbCUx9_4VxMr_GdkC2CiE7OvN6Mh1VmZFNYOECRUYQo130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP700963.RAVbCUx9_4VxMr_GdkC2CiE7OvN6Mh1VmZFNYOECRUYQo130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP700963.RAVbCUx9_4VxMr_GdkC2CiE7OvN6Mh1VmZFNYOECRUYQo130_provenance.
- befree-20150227 importedOn "2015-02-27" NP700963.RAVbCUx9_4VxMr_GdkC2CiE7OvN6Mh1VmZFNYOECRUYQo130_provenance.
- NP700963.RAVbCUx9_4VxMr_GdkC2CiE7OvN6Mh1VmZFNYOECRUYQo130_assertion wasGeneratedBy ECO_0000203 NP700963.RAVbCUx9_4VxMr_GdkC2CiE7OvN6Mh1VmZFNYOECRUYQo130_provenance.
- NP700963.RAVbCUx9_4VxMr_GdkC2CiE7OvN6Mh1VmZFNYOECRUYQo130_assertion wasDerivedFrom befree-20150227 NP700963.RAVbCUx9_4VxMr_GdkC2CiE7OvN6Mh1VmZFNYOECRUYQo130_provenance.
- NP700963.RAVbCUx9_4VxMr_GdkC2CiE7OvN6Mh1VmZFNYOECRUYQo130_assertion SIO_000772 22838948 NP700963.RAVbCUx9_4VxMr_GdkC2CiE7OvN6Mh1VmZFNYOECRUYQo130_provenance.
- NP700963.RAVbCUx9_4VxMr_GdkC2CiE7OvN6Mh1VmZFNYOECRUYQo130_assertion evidence source_evidence_literature NP700963.RAVbCUx9_4VxMr_GdkC2CiE7OvN6Mh1VmZFNYOECRUYQo130_provenance.
- NP700963.RAVbCUx9_4VxMr_GdkC2CiE7OvN6Mh1VmZFNYOECRUYQo130_assertion description "[Children with ALL (n = 96) were screened for GCPII C1561T, RFC1 G80A, cSHMT C1420T, TYMS 5´-UTR 2R3R, TYMS 3´-UTR ins6/del6, MTHFR C677T, MTR A2756G polymorphisms using PCR-RFLP and PCR-amplified fragment length polymorphism techniques.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP700963.RAVbCUx9_4VxMr_GdkC2CiE7OvN6Mh1VmZFNYOECRUYQo130_provenance.