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- source_evidence_literature type ECO_0000212 NP748910.RAds1FIPCurt_jixYWAjNfZXfLVIgMvRObJWiV76xNfaM130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP748910.RAds1FIPCurt_jixYWAjNfZXfLVIgMvRObJWiV76xNfaM130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP748910.RAds1FIPCurt_jixYWAjNfZXfLVIgMvRObJWiV76xNfaM130_provenance.
- NP748910.RAds1FIPCurt_jixYWAjNfZXfLVIgMvRObJWiV76xNfaM130_assertion description "[The existence of the C4A-CYP21P-TNXA/TNXB locus might not be common in CAH patients with 21-hydroxylase deficiency.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP748910.RAds1FIPCurt_jixYWAjNfZXfLVIgMvRObJWiV76xNfaM130_provenance.
- NP748910.RAds1FIPCurt_jixYWAjNfZXfLVIgMvRObJWiV76xNfaM130_assertion evidence source_evidence_literature NP748910.RAds1FIPCurt_jixYWAjNfZXfLVIgMvRObJWiV76xNfaM130_provenance.
- NP748910.RAds1FIPCurt_jixYWAjNfZXfLVIgMvRObJWiV76xNfaM130_assertion SIO_000772 15684714 NP748910.RAds1FIPCurt_jixYWAjNfZXfLVIgMvRObJWiV76xNfaM130_provenance.
- NP748910.RAds1FIPCurt_jixYWAjNfZXfLVIgMvRObJWiV76xNfaM130_assertion wasDerivedFrom befree-20150227 NP748910.RAds1FIPCurt_jixYWAjNfZXfLVIgMvRObJWiV76xNfaM130_provenance.
- NP748910.RAds1FIPCurt_jixYWAjNfZXfLVIgMvRObJWiV76xNfaM130_assertion wasGeneratedBy ECO_0000203 NP748910.RAds1FIPCurt_jixYWAjNfZXfLVIgMvRObJWiV76xNfaM130_provenance.
- befree-20150227 importedOn "2015-02-27" NP748910.RAds1FIPCurt_jixYWAjNfZXfLVIgMvRObJWiV76xNfaM130_provenance.