Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP845862.RAQbhBxGmIbu-T7dbyfDpjuIr1jMcmDZfTj-CfVLg-AMs130_provenance>. }
Showing items 1 to 9 of
9
with 100 items per page.
- source_evidence_literature type ECO_0000212 NP845862.RAQbhBxGmIbu-T7dbyfDpjuIr1jMcmDZfTj-CfVLg-AMs130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP845862.RAQbhBxGmIbu-T7dbyfDpjuIr1jMcmDZfTj-CfVLg-AMs130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP845862.RAQbhBxGmIbu-T7dbyfDpjuIr1jMcmDZfTj-CfVLg-AMs130_provenance.
- NP845862.RAQbhBxGmIbu-T7dbyfDpjuIr1jMcmDZfTj-CfVLg-AMs130_assertion description "[A novel homozygous Arg222Trp missense mutation in WNT7A in two sisters with severe Al-Awadi/Raas-Rothschild/Schinzel phocomelia syndrome.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP845862.RAQbhBxGmIbu-T7dbyfDpjuIr1jMcmDZfTj-CfVLg-AMs130_provenance.
- NP845862.RAQbhBxGmIbu-T7dbyfDpjuIr1jMcmDZfTj-CfVLg-AMs130_assertion evidence source_evidence_literature NP845862.RAQbhBxGmIbu-T7dbyfDpjuIr1jMcmDZfTj-CfVLg-AMs130_provenance.
- NP845862.RAQbhBxGmIbu-T7dbyfDpjuIr1jMcmDZfTj-CfVLg-AMs130_assertion SIO_000772 20949531 NP845862.RAQbhBxGmIbu-T7dbyfDpjuIr1jMcmDZfTj-CfVLg-AMs130_provenance.
- NP845862.RAQbhBxGmIbu-T7dbyfDpjuIr1jMcmDZfTj-CfVLg-AMs130_assertion wasDerivedFrom befree-2016 NP845862.RAQbhBxGmIbu-T7dbyfDpjuIr1jMcmDZfTj-CfVLg-AMs130_provenance.
- NP845862.RAQbhBxGmIbu-T7dbyfDpjuIr1jMcmDZfTj-CfVLg-AMs130_assertion wasGeneratedBy ECO_0000203 NP845862.RAQbhBxGmIbu-T7dbyfDpjuIr1jMcmDZfTj-CfVLg-AMs130_provenance.
- befree-2016 importedOn "2016-02-19" NP845862.RAQbhBxGmIbu-T7dbyfDpjuIr1jMcmDZfTj-CfVLg-AMs130_provenance.