Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP1013311.RAi_zF2H2k4uyEHzxu6IGeHf-zIQ106uGgHV3Cgh5BMmg130_assertion> ?p ?o ?g. }
Showing items 1 to 6 of
6
with 100 items per page.
- NP1013311.RAi_zF2H2k4uyEHzxu6IGeHf-zIQ106uGgHV3Cgh5BMmg130_assertion type Assertion NP1013311.RAi_zF2H2k4uyEHzxu6IGeHf-zIQ106uGgHV3Cgh5BMmg130_head.
- 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.