Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP782275.RAbZGKbt7OoVOW6NnAmH-gWcdPzYZ99CaRiFj18pOTJE0130_provenance>. }
Showing items 1 to 9 of
9
with 100 items per page.
- source_evidence_literature type ECO_0000212 NP782275.RAbZGKbt7OoVOW6NnAmH-gWcdPzYZ99CaRiFj18pOTJE0130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP782275.RAbZGKbt7OoVOW6NnAmH-gWcdPzYZ99CaRiFj18pOTJE0130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP782275.RAbZGKbt7OoVOW6NnAmH-gWcdPzYZ99CaRiFj18pOTJE0130_provenance.
- NP782275.RAbZGKbt7OoVOW6NnAmH-gWcdPzYZ99CaRiFj18pOTJE0130_assertion description "[In addition, we observed that substitution mutations that cause the AVED syndrome impart a marked instability on the TTP protein.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP782275.RAbZGKbt7OoVOW6NnAmH-gWcdPzYZ99CaRiFj18pOTJE0130_provenance.
- NP782275.RAbZGKbt7OoVOW6NnAmH-gWcdPzYZ99CaRiFj18pOTJE0130_assertion evidence source_evidence_literature NP782275.RAbZGKbt7OoVOW6NnAmH-gWcdPzYZ99CaRiFj18pOTJE0130_provenance.
- NP782275.RAbZGKbt7OoVOW6NnAmH-gWcdPzYZ99CaRiFj18pOTJE0130_assertion SIO_000772 16819822 NP782275.RAbZGKbt7OoVOW6NnAmH-gWcdPzYZ99CaRiFj18pOTJE0130_provenance.
- NP782275.RAbZGKbt7OoVOW6NnAmH-gWcdPzYZ99CaRiFj18pOTJE0130_assertion wasDerivedFrom befree-20150227 NP782275.RAbZGKbt7OoVOW6NnAmH-gWcdPzYZ99CaRiFj18pOTJE0130_provenance.
- NP782275.RAbZGKbt7OoVOW6NnAmH-gWcdPzYZ99CaRiFj18pOTJE0130_assertion wasGeneratedBy ECO_0000203 NP782275.RAbZGKbt7OoVOW6NnAmH-gWcdPzYZ99CaRiFj18pOTJE0130_provenance.
- befree-20150227 importedOn "2015-02-27" NP782275.RAbZGKbt7OoVOW6NnAmH-gWcdPzYZ99CaRiFj18pOTJE0130_provenance.