Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP173142.RACUr89X-O5e0N1jYwhpLrQqQfb_QqpfAHv5_nlR2eGl4130_provenance>. }
Showing items 1 to 9 of
9
with 100 items per page.
- source_evidence_literature type ECO_0000212 NP173142.RACUr89X-O5e0N1jYwhpLrQqQfb_QqpfAHv5_nlR2eGl4130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP173142.RACUr89X-O5e0N1jYwhpLrQqQfb_QqpfAHv5_nlR2eGl4130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP173142.RACUr89X-O5e0N1jYwhpLrQqQfb_QqpfAHv5_nlR2eGl4130_provenance.
- NP173142.RACUr89X-O5e0N1jYwhpLrQqQfb_QqpfAHv5_nlR2eGl4130_assertion wasGeneratedBy ECO_0000203 NP173142.RACUr89X-O5e0N1jYwhpLrQqQfb_QqpfAHv5_nlR2eGl4130_provenance.
- NP173142.RACUr89X-O5e0N1jYwhpLrQqQfb_QqpfAHv5_nlR2eGl4130_assertion wasDerivedFrom befree-20140225 NP173142.RACUr89X-O5e0N1jYwhpLrQqQfb_QqpfAHv5_nlR2eGl4130_provenance.
- NP173142.RACUr89X-O5e0N1jYwhpLrQqQfb_QqpfAHv5_nlR2eGl4130_assertion SIO_000772 1773535 NP173142.RACUr89X-O5e0N1jYwhpLrQqQfb_QqpfAHv5_nlR2eGl4130_provenance.
- NP173142.RACUr89X-O5e0N1jYwhpLrQqQfb_QqpfAHv5_nlR2eGl4130_assertion evidence source_evidence_literature NP173142.RACUr89X-O5e0N1jYwhpLrQqQfb_QqpfAHv5_nlR2eGl4130_provenance.
- NP173142.RACUr89X-O5e0N1jYwhpLrQqQfb_QqpfAHv5_nlR2eGl4130_assertion description "[All of them have a balanced reciprocal translocation (46,XY or XX, t(7;9) (q11.21;p12) or (46,XY or XX, t(7;9) (p11.2;q12)), but no other members of the family have either the EEC syndrome or chromosome abnormalities.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP173142.RACUr89X-O5e0N1jYwhpLrQqQfb_QqpfAHv5_nlR2eGl4130_provenance.
- befree-20140225 importedOn "2014-02-25" NP173142.RACUr89X-O5e0N1jYwhpLrQqQfb_QqpfAHv5_nlR2eGl4130_provenance.