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- source_evidence_literature type ECO_0000212 NP540690.RAYDYDHrU6AmVHRLBpiLI0lX9qxqVD8NCi9HuvIrmrgk8130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP540690.RAYDYDHrU6AmVHRLBpiLI0lX9qxqVD8NCi9HuvIrmrgk8130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP540690.RAYDYDHrU6AmVHRLBpiLI0lX9qxqVD8NCi9HuvIrmrgk8130_provenance.
- NP540690.RAYDYDHrU6AmVHRLBpiLI0lX9qxqVD8NCi9HuvIrmrgk8130_assertion description "[Mutation analysis in hereditary haemorrhagic telangiectasia in Germany reveals 11 novel ENG and 12 novel ACVRL1/ALK1 mutations.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP540690.RAYDYDHrU6AmVHRLBpiLI0lX9qxqVD8NCi9HuvIrmrgk8130_provenance.
- NP540690.RAYDYDHrU6AmVHRLBpiLI0lX9qxqVD8NCi9HuvIrmrgk8130_assertion evidence source_evidence_literature NP540690.RAYDYDHrU6AmVHRLBpiLI0lX9qxqVD8NCi9HuvIrmrgk8130_provenance.
- NP540690.RAYDYDHrU6AmVHRLBpiLI0lX9qxqVD8NCi9HuvIrmrgk8130_assertion SIO_000772 16542389 NP540690.RAYDYDHrU6AmVHRLBpiLI0lX9qxqVD8NCi9HuvIrmrgk8130_provenance.
- NP540690.RAYDYDHrU6AmVHRLBpiLI0lX9qxqVD8NCi9HuvIrmrgk8130_assertion wasDerivedFrom befree-2016 NP540690.RAYDYDHrU6AmVHRLBpiLI0lX9qxqVD8NCi9HuvIrmrgk8130_provenance.
- NP540690.RAYDYDHrU6AmVHRLBpiLI0lX9qxqVD8NCi9HuvIrmrgk8130_assertion wasGeneratedBy ECO_0000203 NP540690.RAYDYDHrU6AmVHRLBpiLI0lX9qxqVD8NCi9HuvIrmrgk8130_provenance.
- befree-2016 importedOn "2016-02-19" NP540690.RAYDYDHrU6AmVHRLBpiLI0lX9qxqVD8NCi9HuvIrmrgk8130_provenance.