Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP158893.RANjlk79JWofPkN9SR1wy4Jci5hHfGKOT6I31U5T8Uphk130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP158893.RANjlk79JWofPkN9SR1wy4Jci5hHfGKOT6I31U5T8Uphk130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP158893.RANjlk79JWofPkN9SR1wy4Jci5hHfGKOT6I31U5T8Uphk130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP158893.RANjlk79JWofPkN9SR1wy4Jci5hHfGKOT6I31U5T8Uphk130_provenance.
- NP158893.RANjlk79JWofPkN9SR1wy4Jci5hHfGKOT6I31U5T8Uphk130_assertion description "[The novel finding that WNT16, ST14 and Pcsk1 protein levels increase in fetuses with CHDs suggests that these proteins may play a role in the etiology of human CHDs.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP158893.RANjlk79JWofPkN9SR1wy4Jci5hHfGKOT6I31U5T8Uphk130_provenance.
- NP158893.RANjlk79JWofPkN9SR1wy4Jci5hHfGKOT6I31U5T8Uphk130_assertion evidence source_evidence_literature NP158893.RANjlk79JWofPkN9SR1wy4Jci5hHfGKOT6I31U5T8Uphk130_provenance.
- NP158893.RANjlk79JWofPkN9SR1wy4Jci5hHfGKOT6I31U5T8Uphk130_assertion SIO_000772 19156209 NP158893.RANjlk79JWofPkN9SR1wy4Jci5hHfGKOT6I31U5T8Uphk130_provenance.
- NP158893.RANjlk79JWofPkN9SR1wy4Jci5hHfGKOT6I31U5T8Uphk130_assertion wasDerivedFrom befree-20140225 NP158893.RANjlk79JWofPkN9SR1wy4Jci5hHfGKOT6I31U5T8Uphk130_provenance.
- NP158893.RANjlk79JWofPkN9SR1wy4Jci5hHfGKOT6I31U5T8Uphk130_assertion wasGeneratedBy ECO_0000203 NP158893.RANjlk79JWofPkN9SR1wy4Jci5hHfGKOT6I31U5T8Uphk130_provenance.
- befree-20140225 importedOn "2014-02-25" NP158893.RANjlk79JWofPkN9SR1wy4Jci5hHfGKOT6I31U5T8Uphk130_provenance.