Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP787545.RALMfuf8SzfBvSICYbaEBhrmEu9FS1AW8gqL-v0HC8Gso130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP787545.RALMfuf8SzfBvSICYbaEBhrmEu9FS1AW8gqL-v0HC8Gso130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP787545.RALMfuf8SzfBvSICYbaEBhrmEu9FS1AW8gqL-v0HC8Gso130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP787545.RALMfuf8SzfBvSICYbaEBhrmEu9FS1AW8gqL-v0HC8Gso130_provenance.
- NP787545.RALMfuf8SzfBvSICYbaEBhrmEu9FS1AW8gqL-v0HC8Gso130_assertion description "[We report a mouse model of multiple osteochondromas (MO), an autosomal dominant disease in humans, also known as multiple hereditary exostoses (MHE or HME) and characterized by the formation of cartilage-capped osseous growths projecting from the metaphyses of endochondral bones.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP787545.RALMfuf8SzfBvSICYbaEBhrmEu9FS1AW8gqL-v0HC8Gso130_provenance.
- NP787545.RALMfuf8SzfBvSICYbaEBhrmEu9FS1AW8gqL-v0HC8Gso130_assertion evidence source_evidence_literature NP787545.RALMfuf8SzfBvSICYbaEBhrmEu9FS1AW8gqL-v0HC8Gso130_provenance.
- NP787545.RALMfuf8SzfBvSICYbaEBhrmEu9FS1AW8gqL-v0HC8Gso130_assertion SIO_000772 20080592 NP787545.RALMfuf8SzfBvSICYbaEBhrmEu9FS1AW8gqL-v0HC8Gso130_provenance.
- NP787545.RALMfuf8SzfBvSICYbaEBhrmEu9FS1AW8gqL-v0HC8Gso130_assertion wasDerivedFrom befree-2016 NP787545.RALMfuf8SzfBvSICYbaEBhrmEu9FS1AW8gqL-v0HC8Gso130_provenance.
- NP787545.RALMfuf8SzfBvSICYbaEBhrmEu9FS1AW8gqL-v0HC8Gso130_assertion wasGeneratedBy ECO_0000203 NP787545.RALMfuf8SzfBvSICYbaEBhrmEu9FS1AW8gqL-v0HC8Gso130_provenance.
- befree-2016 importedOn "2016-02-19" NP787545.RALMfuf8SzfBvSICYbaEBhrmEu9FS1AW8gqL-v0HC8Gso130_provenance.