Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP941588.RAjuVeYpue58DFW3xnchGT8Zb_klYzyWkq5iS0GKu_5Sw130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP941588.RAjuVeYpue58DFW3xnchGT8Zb_klYzyWkq5iS0GKu_5Sw130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP941588.RAjuVeYpue58DFW3xnchGT8Zb_klYzyWkq5iS0GKu_5Sw130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP941588.RAjuVeYpue58DFW3xnchGT8Zb_klYzyWkq5iS0GKu_5Sw130_provenance.
- NP941588.RAjuVeYpue58DFW3xnchGT8Zb_klYzyWkq5iS0GKu_5Sw130_assertion description "[Genotypes for ERLIN1, TRAPPC9, and WNK2 may prove informative for assessment of the genetic risk for intracerebral hemorrhage, and those for ITM2C and MAPKAP1 may be beneficial in assessment of the genetic risk for subarachnoid hemorrhage in Japanese individuals.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP941588.RAjuVeYpue58DFW3xnchGT8Zb_klYzyWkq5iS0GKu_5Sw130_provenance.
- NP941588.RAjuVeYpue58DFW3xnchGT8Zb_klYzyWkq5iS0GKu_5Sw130_assertion evidence source_evidence_literature NP941588.RAjuVeYpue58DFW3xnchGT8Zb_klYzyWkq5iS0GKu_5Sw130_provenance.
- NP941588.RAjuVeYpue58DFW3xnchGT8Zb_klYzyWkq5iS0GKu_5Sw130_assertion SIO_000772 20198315 NP941588.RAjuVeYpue58DFW3xnchGT8Zb_klYzyWkq5iS0GKu_5Sw130_provenance.
- NP941588.RAjuVeYpue58DFW3xnchGT8Zb_klYzyWkq5iS0GKu_5Sw130_assertion wasDerivedFrom befree-20150227 NP941588.RAjuVeYpue58DFW3xnchGT8Zb_klYzyWkq5iS0GKu_5Sw130_provenance.
- NP941588.RAjuVeYpue58DFW3xnchGT8Zb_klYzyWkq5iS0GKu_5Sw130_assertion wasGeneratedBy ECO_0000203 NP941588.RAjuVeYpue58DFW3xnchGT8Zb_klYzyWkq5iS0GKu_5Sw130_provenance.
- befree-20150227 importedOn "2015-02-27" NP941588.RAjuVeYpue58DFW3xnchGT8Zb_klYzyWkq5iS0GKu_5Sw130_provenance.