Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP951751.RAaatj2oXMNAtaQo0kMKiLG6zqLE_ncsCF7D9V5wi3450130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP951751.RAaatj2oXMNAtaQo0kMKiLG6zqLE_ncsCF7D9V5wi3450130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP951751.RAaatj2oXMNAtaQo0kMKiLG6zqLE_ncsCF7D9V5wi3450130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP951751.RAaatj2oXMNAtaQo0kMKiLG6zqLE_ncsCF7D9V5wi3450130_provenance.
- NP951751.RAaatj2oXMNAtaQo0kMKiLG6zqLE_ncsCF7D9V5wi3450130_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." NP951751.RAaatj2oXMNAtaQo0kMKiLG6zqLE_ncsCF7D9V5wi3450130_provenance.
- NP951751.RAaatj2oXMNAtaQo0kMKiLG6zqLE_ncsCF7D9V5wi3450130_assertion evidence source_evidence_literature NP951751.RAaatj2oXMNAtaQo0kMKiLG6zqLE_ncsCF7D9V5wi3450130_provenance.
- NP951751.RAaatj2oXMNAtaQo0kMKiLG6zqLE_ncsCF7D9V5wi3450130_assertion SIO_000772 20198315 NP951751.RAaatj2oXMNAtaQo0kMKiLG6zqLE_ncsCF7D9V5wi3450130_provenance.
- NP951751.RAaatj2oXMNAtaQo0kMKiLG6zqLE_ncsCF7D9V5wi3450130_assertion wasDerivedFrom befree-20150227 NP951751.RAaatj2oXMNAtaQo0kMKiLG6zqLE_ncsCF7D9V5wi3450130_provenance.
- NP951751.RAaatj2oXMNAtaQo0kMKiLG6zqLE_ncsCF7D9V5wi3450130_assertion wasGeneratedBy ECO_0000203 NP951751.RAaatj2oXMNAtaQo0kMKiLG6zqLE_ncsCF7D9V5wi3450130_provenance.
- befree-20150227 importedOn "2015-02-27" NP951751.RAaatj2oXMNAtaQo0kMKiLG6zqLE_ncsCF7D9V5wi3450130_provenance.