Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP956031.RABQ8mG0DtKScg0GvkyDB_tA9IpjaNoLtXgGjeAUlxEzw130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP956031.RABQ8mG0DtKScg0GvkyDB_tA9IpjaNoLtXgGjeAUlxEzw130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP956031.RABQ8mG0DtKScg0GvkyDB_tA9IpjaNoLtXgGjeAUlxEzw130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP956031.RABQ8mG0DtKScg0GvkyDB_tA9IpjaNoLtXgGjeAUlxEzw130_provenance.
- befree-20150227 importedOn "2015-02-27" NP956031.RABQ8mG0DtKScg0GvkyDB_tA9IpjaNoLtXgGjeAUlxEzw130_provenance.
- NP956031.RABQ8mG0DtKScg0GvkyDB_tA9IpjaNoLtXgGjeAUlxEzw130_assertion wasGeneratedBy ECO_0000203 NP956031.RABQ8mG0DtKScg0GvkyDB_tA9IpjaNoLtXgGjeAUlxEzw130_provenance.
- NP956031.RABQ8mG0DtKScg0GvkyDB_tA9IpjaNoLtXgGjeAUlxEzw130_assertion wasDerivedFrom befree-20150227 NP956031.RABQ8mG0DtKScg0GvkyDB_tA9IpjaNoLtXgGjeAUlxEzw130_provenance.
- NP956031.RABQ8mG0DtKScg0GvkyDB_tA9IpjaNoLtXgGjeAUlxEzw130_assertion SIO_000772 17220172 NP956031.RABQ8mG0DtKScg0GvkyDB_tA9IpjaNoLtXgGjeAUlxEzw130_provenance.
- NP956031.RABQ8mG0DtKScg0GvkyDB_tA9IpjaNoLtXgGjeAUlxEzw130_assertion evidence source_evidence_literature NP956031.RABQ8mG0DtKScg0GvkyDB_tA9IpjaNoLtXgGjeAUlxEzw130_provenance.
- NP956031.RABQ8mG0DtKScg0GvkyDB_tA9IpjaNoLtXgGjeAUlxEzw130_assertion description "[The Cog8 defect described here represents a novel type of CDG-II, which we propose to name as CDG-IIh or CDG caused by Cog8 deficiency (CDG-II/Cog8).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP956031.RABQ8mG0DtKScg0GvkyDB_tA9IpjaNoLtXgGjeAUlxEzw130_provenance.