Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP828247.RAzyDpn0c-xG4c6puPNtd54_DoBcxyoa84tuFNtpvIJWk130_assertion> ?p ?o ?g. }
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- NP828247.RAzyDpn0c-xG4c6puPNtd54_DoBcxyoa84tuFNtpvIJWk130_assertion type Assertion NP828247.RAzyDpn0c-xG4c6puPNtd54_DoBcxyoa84tuFNtpvIJWk130_head.
- NP828247.RAzyDpn0c-xG4c6puPNtd54_DoBcxyoa84tuFNtpvIJWk130_assertion description "[In addition, we identified a non-synonymous variant in the NKX2-5 gene (P257A) associated with one congenital heart disease patient with VSD.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP828247.RAzyDpn0c-xG4c6puPNtd54_DoBcxyoa84tuFNtpvIJWk130_provenance.
- NP828247.RAzyDpn0c-xG4c6puPNtd54_DoBcxyoa84tuFNtpvIJWk130_assertion evidence source_evidence_literature NP828247.RAzyDpn0c-xG4c6puPNtd54_DoBcxyoa84tuFNtpvIJWk130_provenance.
- NP828247.RAzyDpn0c-xG4c6puPNtd54_DoBcxyoa84tuFNtpvIJWk130_assertion SIO_000772 20659440 NP828247.RAzyDpn0c-xG4c6puPNtd54_DoBcxyoa84tuFNtpvIJWk130_provenance.
- NP828247.RAzyDpn0c-xG4c6puPNtd54_DoBcxyoa84tuFNtpvIJWk130_assertion wasDerivedFrom befree-2016 NP828247.RAzyDpn0c-xG4c6puPNtd54_DoBcxyoa84tuFNtpvIJWk130_provenance.
- NP828247.RAzyDpn0c-xG4c6puPNtd54_DoBcxyoa84tuFNtpvIJWk130_assertion wasGeneratedBy ECO_0000203 NP828247.RAzyDpn0c-xG4c6puPNtd54_DoBcxyoa84tuFNtpvIJWk130_provenance.