Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP726563.RAEj7EbOe4wqJBAG0tp6SGVhNEOwR01E_umHIalegF8fw130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP726563.RAEj7EbOe4wqJBAG0tp6SGVhNEOwR01E_umHIalegF8fw130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP726563.RAEj7EbOe4wqJBAG0tp6SGVhNEOwR01E_umHIalegF8fw130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP726563.RAEj7EbOe4wqJBAG0tp6SGVhNEOwR01E_umHIalegF8fw130_provenance.
- NP726563.RAEj7EbOe4wqJBAG0tp6SGVhNEOwR01E_umHIalegF8fw130_assertion description "[Molecular and cytogenetic analysis in two patients with microdeletions of 7p and Greig syndrome: hemizygosity for PGAM2 and TCRG genes.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP726563.RAEj7EbOe4wqJBAG0tp6SGVhNEOwR01E_umHIalegF8fw130_provenance.
- NP726563.RAEj7EbOe4wqJBAG0tp6SGVhNEOwR01E_umHIalegF8fw130_assertion evidence source_evidence_literature NP726563.RAEj7EbOe4wqJBAG0tp6SGVhNEOwR01E_umHIalegF8fw130_provenance.
- NP726563.RAEj7EbOe4wqJBAG0tp6SGVhNEOwR01E_umHIalegF8fw130_assertion SIO_000772 1981052 NP726563.RAEj7EbOe4wqJBAG0tp6SGVhNEOwR01E_umHIalegF8fw130_provenance.
- NP726563.RAEj7EbOe4wqJBAG0tp6SGVhNEOwR01E_umHIalegF8fw130_assertion wasDerivedFrom befree-20150227 NP726563.RAEj7EbOe4wqJBAG0tp6SGVhNEOwR01E_umHIalegF8fw130_provenance.
- NP726563.RAEj7EbOe4wqJBAG0tp6SGVhNEOwR01E_umHIalegF8fw130_assertion wasGeneratedBy ECO_0000203 NP726563.RAEj7EbOe4wqJBAG0tp6SGVhNEOwR01E_umHIalegF8fw130_provenance.
- befree-20150227 importedOn "2015-02-27" NP726563.RAEj7EbOe4wqJBAG0tp6SGVhNEOwR01E_umHIalegF8fw130_provenance.