Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP1013311.RAi_zF2H2k4uyEHzxu6IGeHf-zIQ106uGgHV3Cgh5BMmg130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP1013311.RAi_zF2H2k4uyEHzxu6IGeHf-zIQ106uGgHV3Cgh5BMmg130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP1013311.RAi_zF2H2k4uyEHzxu6IGeHf-zIQ106uGgHV3Cgh5BMmg130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP1013311.RAi_zF2H2k4uyEHzxu6IGeHf-zIQ106uGgHV3Cgh5BMmg130_provenance.
- befree-20150227 importedOn "2015-02-27" NP1013311.RAi_zF2H2k4uyEHzxu6IGeHf-zIQ106uGgHV3Cgh5BMmg130_provenance.
- NP1013311.RAi_zF2H2k4uyEHzxu6IGeHf-zIQ106uGgHV3Cgh5BMmg130_assertion wasGeneratedBy ECO_0000203 NP1013311.RAi_zF2H2k4uyEHzxu6IGeHf-zIQ106uGgHV3Cgh5BMmg130_provenance.
- NP1013311.RAi_zF2H2k4uyEHzxu6IGeHf-zIQ106uGgHV3Cgh5BMmg130_assertion wasDerivedFrom befree-20150227 NP1013311.RAi_zF2H2k4uyEHzxu6IGeHf-zIQ106uGgHV3Cgh5BMmg130_provenance.
- NP1013311.RAi_zF2H2k4uyEHzxu6IGeHf-zIQ106uGgHV3Cgh5BMmg130_assertion SIO_000772 22578324 NP1013311.RAi_zF2H2k4uyEHzxu6IGeHf-zIQ106uGgHV3Cgh5BMmg130_provenance.
- NP1013311.RAi_zF2H2k4uyEHzxu6IGeHf-zIQ106uGgHV3Cgh5BMmg130_assertion evidence source_evidence_literature NP1013311.RAi_zF2H2k4uyEHzxu6IGeHf-zIQ106uGgHV3Cgh5BMmg130_provenance.
- NP1013311.RAi_zF2H2k4uyEHzxu6IGeHf-zIQ106uGgHV3Cgh5BMmg130_assertion description "[Duplication (dup7q11.23) and deletion (Williams syndrome) of chromosomal region 7q11.23 cause neurodevelopmental disorders with contrasting anxiety phenotypes.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1013311.RAi_zF2H2k4uyEHzxu6IGeHf-zIQ106uGgHV3Cgh5BMmg130_provenance.