Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP1323191.RA2lsqP7IHoYmFFapcrVHv0s-jr4F6aEezVeX6XT9Gzos130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP1323191.RA2lsqP7IHoYmFFapcrVHv0s-jr4F6aEezVeX6XT9Gzos130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP1323191.RA2lsqP7IHoYmFFapcrVHv0s-jr4F6aEezVeX6XT9Gzos130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP1323191.RA2lsqP7IHoYmFFapcrVHv0s-jr4F6aEezVeX6XT9Gzos130_provenance.
- befree-2016 importedOn "2016-02-19" NP1323191.RA2lsqP7IHoYmFFapcrVHv0s-jr4F6aEezVeX6XT9Gzos130_provenance.
- NP1323191.RA2lsqP7IHoYmFFapcrVHv0s-jr4F6aEezVeX6XT9Gzos130_assertion wasGeneratedBy ECO_0000203 NP1323191.RA2lsqP7IHoYmFFapcrVHv0s-jr4F6aEezVeX6XT9Gzos130_provenance.
- NP1323191.RA2lsqP7IHoYmFFapcrVHv0s-jr4F6aEezVeX6XT9Gzos130_assertion wasDerivedFrom befree-2016 NP1323191.RA2lsqP7IHoYmFFapcrVHv0s-jr4F6aEezVeX6XT9Gzos130_provenance.
- NP1323191.RA2lsqP7IHoYmFFapcrVHv0s-jr4F6aEezVeX6XT9Gzos130_assertion SIO_000772 7829628 NP1323191.RA2lsqP7IHoYmFFapcrVHv0s-jr4F6aEezVeX6XT9Gzos130_provenance.
- NP1323191.RA2lsqP7IHoYmFFapcrVHv0s-jr4F6aEezVeX6XT9Gzos130_assertion evidence source_evidence_literature NP1323191.RA2lsqP7IHoYmFFapcrVHv0s-jr4F6aEezVeX6XT9Gzos130_provenance.
- NP1323191.RA2lsqP7IHoYmFFapcrVHv0s-jr4F6aEezVeX6XT9Gzos130_assertion description "[DNA sequence analysis showed that none of the affected individuals had mutations in either exon 10 or 11, or in exon 16 of the RET protooncogene, regions where mutations have been described for MEN type 2A (MEN-2A) and MEN-2B families, respectively.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1323191.RA2lsqP7IHoYmFFapcrVHv0s-jr4F6aEezVeX6XT9Gzos130_provenance.