Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP361939.RAYJXaPzSTG1NmQFFn6eQOeMLeCBQ_Va6NN-XoTQTs_DE130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP361939.RAYJXaPzSTG1NmQFFn6eQOeMLeCBQ_Va6NN-XoTQTs_DE130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP361939.RAYJXaPzSTG1NmQFFn6eQOeMLeCBQ_Va6NN-XoTQTs_DE130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP361939.RAYJXaPzSTG1NmQFFn6eQOeMLeCBQ_Va6NN-XoTQTs_DE130_provenance.
- NP361939.RAYJXaPzSTG1NmQFFn6eQOeMLeCBQ_Va6NN-XoTQTs_DE130_assertion description "[Dentinogenesis imperfecta 1 (DGI1, MIM 125490) is an autosomal dominant dental disease characterized by abnormal dentin production and mineralization.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP361939.RAYJXaPzSTG1NmQFFn6eQOeMLeCBQ_Va6NN-XoTQTs_DE130_provenance.
- NP361939.RAYJXaPzSTG1NmQFFn6eQOeMLeCBQ_Va6NN-XoTQTs_DE130_assertion evidence source_evidence_literature NP361939.RAYJXaPzSTG1NmQFFn6eQOeMLeCBQ_Va6NN-XoTQTs_DE130_provenance.
- NP361939.RAYJXaPzSTG1NmQFFn6eQOeMLeCBQ_Va6NN-XoTQTs_DE130_assertion SIO_000772 11175790 NP361939.RAYJXaPzSTG1NmQFFn6eQOeMLeCBQ_Va6NN-XoTQTs_DE130_provenance.
- NP361939.RAYJXaPzSTG1NmQFFn6eQOeMLeCBQ_Va6NN-XoTQTs_DE130_assertion wasDerivedFrom befree-20150227 NP361939.RAYJXaPzSTG1NmQFFn6eQOeMLeCBQ_Va6NN-XoTQTs_DE130_provenance.
- NP361939.RAYJXaPzSTG1NmQFFn6eQOeMLeCBQ_Va6NN-XoTQTs_DE130_assertion wasGeneratedBy ECO_0000203 NP361939.RAYJXaPzSTG1NmQFFn6eQOeMLeCBQ_Va6NN-XoTQTs_DE130_provenance.
- befree-20150227 importedOn "2015-02-27" NP361939.RAYJXaPzSTG1NmQFFn6eQOeMLeCBQ_Va6NN-XoTQTs_DE130_provenance.