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- source_evidence_literature type ECO_0000212 NP811125.RAqM2quBszHW5UD_F582WgUPeq5CokU1XabZaXb01EWHA130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP811125.RAqM2quBszHW5UD_F582WgUPeq5CokU1XabZaXb01EWHA130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP811125.RAqM2quBszHW5UD_F582WgUPeq5CokU1XabZaXb01EWHA130_provenance.
- 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.
- befree-2016 importedOn "2016-02-19" NP811125.RAqM2quBszHW5UD_F582WgUPeq5CokU1XabZaXb01EWHA130_provenance.