Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP361886.RABqvLaotip6OpaJrfQi6HIc08BegoPwouf7JF_uaHL1U130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP361886.RABqvLaotip6OpaJrfQi6HIc08BegoPwouf7JF_uaHL1U130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP361886.RABqvLaotip6OpaJrfQi6HIc08BegoPwouf7JF_uaHL1U130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP361886.RABqvLaotip6OpaJrfQi6HIc08BegoPwouf7JF_uaHL1U130_provenance.
- befree-20150227 importedOn "2015-02-27" NP361886.RABqvLaotip6OpaJrfQi6HIc08BegoPwouf7JF_uaHL1U130_provenance.
- NP361886.RABqvLaotip6OpaJrfQi6HIc08BegoPwouf7JF_uaHL1U130_assertion wasGeneratedBy ECO_0000203 NP361886.RABqvLaotip6OpaJrfQi6HIc08BegoPwouf7JF_uaHL1U130_provenance.
- NP361886.RABqvLaotip6OpaJrfQi6HIc08BegoPwouf7JF_uaHL1U130_assertion wasDerivedFrom befree-20150227 NP361886.RABqvLaotip6OpaJrfQi6HIc08BegoPwouf7JF_uaHL1U130_provenance.
- NP361886.RABqvLaotip6OpaJrfQi6HIc08BegoPwouf7JF_uaHL1U130_assertion SIO_000772 22521702 NP361886.RABqvLaotip6OpaJrfQi6HIc08BegoPwouf7JF_uaHL1U130_provenance.
- NP361886.RABqvLaotip6OpaJrfQi6HIc08BegoPwouf7JF_uaHL1U130_assertion evidence source_evidence_literature NP361886.RABqvLaotip6OpaJrfQi6HIc08BegoPwouf7JF_uaHL1U130_provenance.
- NP361886.RABqvLaotip6OpaJrfQi6HIc08BegoPwouf7JF_uaHL1U130_assertion description "[Hereditary dentine disorders dentinogenesis imperfecta type II/III and dentine dysplasia are currently proposed to be one disease with distinct clinical manifestations reflecting various mutations in the same DSPP gene.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP361886.RABqvLaotip6OpaJrfQi6HIc08BegoPwouf7JF_uaHL1U130_provenance.