Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP791949.RAyUndkmO9uivcSv4QoLyy6JjWRX8Gd-Tw0VMZp5qvXVA130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP791949.RAyUndkmO9uivcSv4QoLyy6JjWRX8Gd-Tw0VMZp5qvXVA130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP791949.RAyUndkmO9uivcSv4QoLyy6JjWRX8Gd-Tw0VMZp5qvXVA130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP791949.RAyUndkmO9uivcSv4QoLyy6JjWRX8Gd-Tw0VMZp5qvXVA130_provenance.
- NP791949.RAyUndkmO9uivcSv4QoLyy6JjWRX8Gd-Tw0VMZp5qvXVA130_assertion description "[Identification of a novel causative mutation in the ROR2 gene in a Lebanese family with a mild form of recessive Robinow syndrome.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP791949.RAyUndkmO9uivcSv4QoLyy6JjWRX8Gd-Tw0VMZp5qvXVA130_provenance.
- NP791949.RAyUndkmO9uivcSv4QoLyy6JjWRX8Gd-Tw0VMZp5qvXVA130_assertion evidence source_evidence_literature NP791949.RAyUndkmO9uivcSv4QoLyy6JjWRX8Gd-Tw0VMZp5qvXVA130_provenance.
- NP791949.RAyUndkmO9uivcSv4QoLyy6JjWRX8Gd-Tw0VMZp5qvXVA130_assertion SIO_000772 22178368 NP791949.RAyUndkmO9uivcSv4QoLyy6JjWRX8Gd-Tw0VMZp5qvXVA130_provenance.
- NP791949.RAyUndkmO9uivcSv4QoLyy6JjWRX8Gd-Tw0VMZp5qvXVA130_assertion wasDerivedFrom befree-20140225 NP791949.RAyUndkmO9uivcSv4QoLyy6JjWRX8Gd-Tw0VMZp5qvXVA130_provenance.
- NP791949.RAyUndkmO9uivcSv4QoLyy6JjWRX8Gd-Tw0VMZp5qvXVA130_assertion wasGeneratedBy ECO_0000203 NP791949.RAyUndkmO9uivcSv4QoLyy6JjWRX8Gd-Tw0VMZp5qvXVA130_provenance.
- befree-20140225 importedOn "2014-02-25" NP791949.RAyUndkmO9uivcSv4QoLyy6JjWRX8Gd-Tw0VMZp5qvXVA130_provenance.