Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP1021941.RABy9EzizwS-jUIFZcuiLDgV99OQ5HcJrUWTlL_zDSdys130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP1021941.RABy9EzizwS-jUIFZcuiLDgV99OQ5HcJrUWTlL_zDSdys130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP1021941.RABy9EzizwS-jUIFZcuiLDgV99OQ5HcJrUWTlL_zDSdys130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP1021941.RABy9EzizwS-jUIFZcuiLDgV99OQ5HcJrUWTlL_zDSdys130_provenance.
- befree-2016 importedOn "2016-02-19" NP1021941.RABy9EzizwS-jUIFZcuiLDgV99OQ5HcJrUWTlL_zDSdys130_provenance.
- NP1021941.RABy9EzizwS-jUIFZcuiLDgV99OQ5HcJrUWTlL_zDSdys130_assertion wasGeneratedBy ECO_0000203 NP1021941.RABy9EzizwS-jUIFZcuiLDgV99OQ5HcJrUWTlL_zDSdys130_provenance.
- NP1021941.RABy9EzizwS-jUIFZcuiLDgV99OQ5HcJrUWTlL_zDSdys130_assertion wasDerivedFrom befree-2016 NP1021941.RABy9EzizwS-jUIFZcuiLDgV99OQ5HcJrUWTlL_zDSdys130_provenance.
- NP1021941.RABy9EzizwS-jUIFZcuiLDgV99OQ5HcJrUWTlL_zDSdys130_assertion SIO_000772 23076529 NP1021941.RABy9EzizwS-jUIFZcuiLDgV99OQ5HcJrUWTlL_zDSdys130_provenance.
- NP1021941.RABy9EzizwS-jUIFZcuiLDgV99OQ5HcJrUWTlL_zDSdys130_assertion evidence source_evidence_literature NP1021941.RABy9EzizwS-jUIFZcuiLDgV99OQ5HcJrUWTlL_zDSdys130_provenance.
- NP1021941.RABy9EzizwS-jUIFZcuiLDgV99OQ5HcJrUWTlL_zDSdys130_assertion description "[There is evidence suggesting that genetic variants of Nodal signaling may be associated with risk of congenital heart diseases (CHDs), in which several polymorphisms, such as Nodal rs1904589, have been considered to be implicated in the accumulation of the genetic burden of CHD risk with interacting genes.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1021941.RABy9EzizwS-jUIFZcuiLDgV99OQ5HcJrUWTlL_zDSdys130_provenance.