Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP918857.RAAI-CFGcPiwp6qBXC9dU4N7VpRP2qNzgOyCY7cMiS-wA130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP918857.RAAI-CFGcPiwp6qBXC9dU4N7VpRP2qNzgOyCY7cMiS-wA130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP918857.RAAI-CFGcPiwp6qBXC9dU4N7VpRP2qNzgOyCY7cMiS-wA130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP918857.RAAI-CFGcPiwp6qBXC9dU4N7VpRP2qNzgOyCY7cMiS-wA130_provenance.
- NP918857.RAAI-CFGcPiwp6qBXC9dU4N7VpRP2qNzgOyCY7cMiS-wA130_assertion description "[Identification of ADAMTS18 as a gene mutated in Knobloch syndrome.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP918857.RAAI-CFGcPiwp6qBXC9dU4N7VpRP2qNzgOyCY7cMiS-wA130_provenance.
- NP918857.RAAI-CFGcPiwp6qBXC9dU4N7VpRP2qNzgOyCY7cMiS-wA130_assertion evidence source_evidence_literature NP918857.RAAI-CFGcPiwp6qBXC9dU4N7VpRP2qNzgOyCY7cMiS-wA130_provenance.
- NP918857.RAAI-CFGcPiwp6qBXC9dU4N7VpRP2qNzgOyCY7cMiS-wA130_assertion SIO_000772 21862674 NP918857.RAAI-CFGcPiwp6qBXC9dU4N7VpRP2qNzgOyCY7cMiS-wA130_provenance.
- NP918857.RAAI-CFGcPiwp6qBXC9dU4N7VpRP2qNzgOyCY7cMiS-wA130_assertion wasDerivedFrom befree-2016 NP918857.RAAI-CFGcPiwp6qBXC9dU4N7VpRP2qNzgOyCY7cMiS-wA130_provenance.
- NP918857.RAAI-CFGcPiwp6qBXC9dU4N7VpRP2qNzgOyCY7cMiS-wA130_assertion wasGeneratedBy ECO_0000203 NP918857.RAAI-CFGcPiwp6qBXC9dU4N7VpRP2qNzgOyCY7cMiS-wA130_provenance.
- befree-2016 importedOn "2016-02-19" NP918857.RAAI-CFGcPiwp6qBXC9dU4N7VpRP2qNzgOyCY7cMiS-wA130_provenance.