Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP418859.RAEPVlUuL2b5Rc_HKU7ZxVAY0HMF_XEL4Jlfk1LuHVFsU130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP418859.RAEPVlUuL2b5Rc_HKU7ZxVAY0HMF_XEL4Jlfk1LuHVFsU130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP418859.RAEPVlUuL2b5Rc_HKU7ZxVAY0HMF_XEL4Jlfk1LuHVFsU130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP418859.RAEPVlUuL2b5Rc_HKU7ZxVAY0HMF_XEL4Jlfk1LuHVFsU130_provenance.
- befree-20150227 importedOn "2015-02-27" NP418859.RAEPVlUuL2b5Rc_HKU7ZxVAY0HMF_XEL4Jlfk1LuHVFsU130_provenance.
- NP418859.RAEPVlUuL2b5Rc_HKU7ZxVAY0HMF_XEL4Jlfk1LuHVFsU130_assertion wasGeneratedBy ECO_0000203 NP418859.RAEPVlUuL2b5Rc_HKU7ZxVAY0HMF_XEL4Jlfk1LuHVFsU130_provenance.
- NP418859.RAEPVlUuL2b5Rc_HKU7ZxVAY0HMF_XEL4Jlfk1LuHVFsU130_assertion wasDerivedFrom befree-20150227 NP418859.RAEPVlUuL2b5Rc_HKU7ZxVAY0HMF_XEL4Jlfk1LuHVFsU130_provenance.
- NP418859.RAEPVlUuL2b5Rc_HKU7ZxVAY0HMF_XEL4Jlfk1LuHVFsU130_assertion SIO_000772 25035146 NP418859.RAEPVlUuL2b5Rc_HKU7ZxVAY0HMF_XEL4Jlfk1LuHVFsU130_provenance.
- NP418859.RAEPVlUuL2b5Rc_HKU7ZxVAY0HMF_XEL4Jlfk1LuHVFsU130_assertion evidence source_evidence_literature NP418859.RAEPVlUuL2b5Rc_HKU7ZxVAY0HMF_XEL4Jlfk1LuHVFsU130_provenance.
- NP418859.RAEPVlUuL2b5Rc_HKU7ZxVAY0HMF_XEL4Jlfk1LuHVFsU130_assertion description "[In this issue of Blood, Gagne et al describe a cohort of 362 patients clinically classified as having Diamond-Blackfan anemia (DBA), in which 175 (48%) were found to have mutations and deletions in ribosomal protein genes or GATA1, and 8 of the remaining patients (2.2% overall) had mitochondrial gene deletions consistent with Pearson marrow-pancreas syndrome (PS).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP418859.RAEPVlUuL2b5Rc_HKU7ZxVAY0HMF_XEL4Jlfk1LuHVFsU130_provenance.