Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP463424.RAfD2sQo7LiPmiE5hNUZzGMl190ooPs11bR1lNWDBx67k130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP463424.RAfD2sQo7LiPmiE5hNUZzGMl190ooPs11bR1lNWDBx67k130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP463424.RAfD2sQo7LiPmiE5hNUZzGMl190ooPs11bR1lNWDBx67k130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP463424.RAfD2sQo7LiPmiE5hNUZzGMl190ooPs11bR1lNWDBx67k130_provenance.
- NP463424.RAfD2sQo7LiPmiE5hNUZzGMl190ooPs11bR1lNWDBx67k130_assertion description "[Family-based association study of DYX1C1 variants in autism.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP463424.RAfD2sQo7LiPmiE5hNUZzGMl190ooPs11bR1lNWDBx67k130_provenance.
- NP463424.RAfD2sQo7LiPmiE5hNUZzGMl190ooPs11bR1lNWDBx67k130_assertion evidence source_evidence_literature NP463424.RAfD2sQo7LiPmiE5hNUZzGMl190ooPs11bR1lNWDBx67k130_provenance.
- NP463424.RAfD2sQo7LiPmiE5hNUZzGMl190ooPs11bR1lNWDBx67k130_assertion SIO_000772 15470369 NP463424.RAfD2sQo7LiPmiE5hNUZzGMl190ooPs11bR1lNWDBx67k130_provenance.
- NP463424.RAfD2sQo7LiPmiE5hNUZzGMl190ooPs11bR1lNWDBx67k130_assertion wasDerivedFrom befree-2016 NP463424.RAfD2sQo7LiPmiE5hNUZzGMl190ooPs11bR1lNWDBx67k130_provenance.
- NP463424.RAfD2sQo7LiPmiE5hNUZzGMl190ooPs11bR1lNWDBx67k130_assertion wasGeneratedBy ECO_0000203 NP463424.RAfD2sQo7LiPmiE5hNUZzGMl190ooPs11bR1lNWDBx67k130_provenance.
- befree-2016 importedOn "2016-02-19" NP463424.RAfD2sQo7LiPmiE5hNUZzGMl190ooPs11bR1lNWDBx67k130_provenance.