Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP811125.RAqM2quBszHW5UD_F582WgUPeq5CokU1XabZaXb01EWHA130_assertion> ?p ?o ?g. }
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- NP811125.RAqM2quBszHW5UD_F582WgUPeq5CokU1XabZaXb01EWHA130_assertion type Assertion NP811125.RAqM2quBszHW5UD_F582WgUPeq5CokU1XabZaXb01EWHA130_head.
- NP811125.RAqM2quBszHW5UD_F582WgUPeq5CokU1XabZaXb01EWHA130_assertion description "[Thus, even important for cardiac development, germline mutations in NKX2.5 are rare in patients with sporadic CHD and genetic and/or pathophysiologic heterogeneity is likely for sporadic forms of CHD.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP811125.RAqM2quBszHW5UD_F582WgUPeq5CokU1XabZaXb01EWHA130_provenance.
- NP811125.RAqM2quBszHW5UD_F582WgUPeq5CokU1XabZaXb01EWHA130_assertion evidence source_evidence_literature NP811125.RAqM2quBszHW5UD_F582WgUPeq5CokU1XabZaXb01EWHA130_provenance.
- NP811125.RAqM2quBszHW5UD_F582WgUPeq5CokU1XabZaXb01EWHA130_assertion SIO_000772 20456451 NP811125.RAqM2quBszHW5UD_F582WgUPeq5CokU1XabZaXb01EWHA130_provenance.
- NP811125.RAqM2quBszHW5UD_F582WgUPeq5CokU1XabZaXb01EWHA130_assertion wasDerivedFrom befree-2016 NP811125.RAqM2quBszHW5UD_F582WgUPeq5CokU1XabZaXb01EWHA130_provenance.
- NP811125.RAqM2quBszHW5UD_F582WgUPeq5CokU1XabZaXb01EWHA130_assertion wasGeneratedBy ECO_0000203 NP811125.RAqM2quBszHW5UD_F582WgUPeq5CokU1XabZaXb01EWHA130_provenance.