Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP200889.RAPWj_H1e_vQ3d39B3of3uhaRU5kwIpi798ewARvx5Wlo130_provenance>. }
Showing items 1 to 9 of
9
with 100 items per page.
- source_evidence_literature type ECO_0000212 NP200889.RAPWj_H1e_vQ3d39B3of3uhaRU5kwIpi798ewARvx5Wlo130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP200889.RAPWj_H1e_vQ3d39B3of3uhaRU5kwIpi798ewARvx5Wlo130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP200889.RAPWj_H1e_vQ3d39B3of3uhaRU5kwIpi798ewARvx5Wlo130_provenance.
- NP200889.RAPWj_H1e_vQ3d39B3of3uhaRU5kwIpi798ewARvx5Wlo130_assertion description "[Mutations in kelch-like 3 (KLHL3) and Cullin3 were also recently identified as causing PHAII.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP200889.RAPWj_H1e_vQ3d39B3of3uhaRU5kwIpi798ewARvx5Wlo130_provenance.
- NP200889.RAPWj_H1e_vQ3d39B3of3uhaRU5kwIpi798ewARvx5Wlo130_assertion evidence source_evidence_literature NP200889.RAPWj_H1e_vQ3d39B3of3uhaRU5kwIpi798ewARvx5Wlo130_provenance.
- NP200889.RAPWj_H1e_vQ3d39B3of3uhaRU5kwIpi798ewARvx5Wlo130_assertion SIO_000772 23453970 NP200889.RAPWj_H1e_vQ3d39B3of3uhaRU5kwIpi798ewARvx5Wlo130_provenance.
- NP200889.RAPWj_H1e_vQ3d39B3of3uhaRU5kwIpi798ewARvx5Wlo130_assertion wasDerivedFrom befree-20140225 NP200889.RAPWj_H1e_vQ3d39B3of3uhaRU5kwIpi798ewARvx5Wlo130_provenance.
- NP200889.RAPWj_H1e_vQ3d39B3of3uhaRU5kwIpi798ewARvx5Wlo130_assertion wasGeneratedBy ECO_0000203 NP200889.RAPWj_H1e_vQ3d39B3of3uhaRU5kwIpi798ewARvx5Wlo130_provenance.
- befree-20140225 importedOn "2014-02-25" NP200889.RAPWj_H1e_vQ3d39B3of3uhaRU5kwIpi798ewARvx5Wlo130_provenance.