Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP859414.RAC6np-5BFz8mGgqkJD_LnPQxEznCu-8De7oivXfVrlzQ130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP859414.RAC6np-5BFz8mGgqkJD_LnPQxEznCu-8De7oivXfVrlzQ130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP859414.RAC6np-5BFz8mGgqkJD_LnPQxEznCu-8De7oivXfVrlzQ130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP859414.RAC6np-5BFz8mGgqkJD_LnPQxEznCu-8De7oivXfVrlzQ130_provenance.
- NP859414.RAC6np-5BFz8mGgqkJD_LnPQxEznCu-8De7oivXfVrlzQ130_assertion description "[OI type V has an autosomal-dominant pattern of inheritance and is not caused by mutations in the type I collagen genes COL1A1 and COL1A2.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP859414.RAC6np-5BFz8mGgqkJD_LnPQxEznCu-8De7oivXfVrlzQ130_provenance.
- NP859414.RAC6np-5BFz8mGgqkJD_LnPQxEznCu-8De7oivXfVrlzQ130_assertion evidence source_evidence_literature NP859414.RAC6np-5BFz8mGgqkJD_LnPQxEznCu-8De7oivXfVrlzQ130_provenance.
- NP859414.RAC6np-5BFz8mGgqkJD_LnPQxEznCu-8De7oivXfVrlzQ130_assertion SIO_000772 22863195 NP859414.RAC6np-5BFz8mGgqkJD_LnPQxEznCu-8De7oivXfVrlzQ130_provenance.
- NP859414.RAC6np-5BFz8mGgqkJD_LnPQxEznCu-8De7oivXfVrlzQ130_assertion wasDerivedFrom befree-20140225 NP859414.RAC6np-5BFz8mGgqkJD_LnPQxEznCu-8De7oivXfVrlzQ130_provenance.
- NP859414.RAC6np-5BFz8mGgqkJD_LnPQxEznCu-8De7oivXfVrlzQ130_assertion wasGeneratedBy ECO_0000203 NP859414.RAC6np-5BFz8mGgqkJD_LnPQxEznCu-8De7oivXfVrlzQ130_provenance.
- befree-20140225 importedOn "2014-02-25" NP859414.RAC6np-5BFz8mGgqkJD_LnPQxEznCu-8De7oivXfVrlzQ130_provenance.