Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP350698.RAQZ_SF15nnecqHsni0m7FHdy9eN8UbcbfFdGNBZrTdCU130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP350698.RAQZ_SF15nnecqHsni0m7FHdy9eN8UbcbfFdGNBZrTdCU130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP350698.RAQZ_SF15nnecqHsni0m7FHdy9eN8UbcbfFdGNBZrTdCU130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP350698.RAQZ_SF15nnecqHsni0m7FHdy9eN8UbcbfFdGNBZrTdCU130_provenance.
- NP350698.RAQZ_SF15nnecqHsni0m7FHdy9eN8UbcbfFdGNBZrTdCU130_assertion description "[Four neonates whose mothers were affected by AT III congenital defect were also investigated: diagnosis of congenital deficiency was established in three cases.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP350698.RAQZ_SF15nnecqHsni0m7FHdy9eN8UbcbfFdGNBZrTdCU130_provenance.
- NP350698.RAQZ_SF15nnecqHsni0m7FHdy9eN8UbcbfFdGNBZrTdCU130_assertion evidence source_evidence_literature NP350698.RAQZ_SF15nnecqHsni0m7FHdy9eN8UbcbfFdGNBZrTdCU130_provenance.
- NP350698.RAQZ_SF15nnecqHsni0m7FHdy9eN8UbcbfFdGNBZrTdCU130_assertion SIO_000772 3660333 NP350698.RAQZ_SF15nnecqHsni0m7FHdy9eN8UbcbfFdGNBZrTdCU130_provenance.
- NP350698.RAQZ_SF15nnecqHsni0m7FHdy9eN8UbcbfFdGNBZrTdCU130_assertion wasDerivedFrom befree-20140225 NP350698.RAQZ_SF15nnecqHsni0m7FHdy9eN8UbcbfFdGNBZrTdCU130_provenance.
- NP350698.RAQZ_SF15nnecqHsni0m7FHdy9eN8UbcbfFdGNBZrTdCU130_assertion wasGeneratedBy ECO_0000203 NP350698.RAQZ_SF15nnecqHsni0m7FHdy9eN8UbcbfFdGNBZrTdCU130_provenance.
- befree-20140225 importedOn "2014-02-25" NP350698.RAQZ_SF15nnecqHsni0m7FHdy9eN8UbcbfFdGNBZrTdCU130_provenance.