Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP827878.RAtVGwxqCiSW_L_W11HhPcKh7w2JmiPYXIXZMZmU4HEFY130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP827878.RAtVGwxqCiSW_L_W11HhPcKh7w2JmiPYXIXZMZmU4HEFY130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP827878.RAtVGwxqCiSW_L_W11HhPcKh7w2JmiPYXIXZMZmU4HEFY130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP827878.RAtVGwxqCiSW_L_W11HhPcKh7w2JmiPYXIXZMZmU4HEFY130_provenance.
- NP827878.RAtVGwxqCiSW_L_W11HhPcKh7w2JmiPYXIXZMZmU4HEFY130_assertion description "[MECP2 coding sequence and 3'UTR variation in 172 unrelated autistic patients.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP827878.RAtVGwxqCiSW_L_W11HhPcKh7w2JmiPYXIXZMZmU4HEFY130_provenance.
- NP827878.RAtVGwxqCiSW_L_W11HhPcKh7w2JmiPYXIXZMZmU4HEFY130_assertion evidence source_evidence_literature NP827878.RAtVGwxqCiSW_L_W11HhPcKh7w2JmiPYXIXZMZmU4HEFY130_provenance.
- NP827878.RAtVGwxqCiSW_L_W11HhPcKh7w2JmiPYXIXZMZmU4HEFY130_assertion SIO_000772 17427193 NP827878.RAtVGwxqCiSW_L_W11HhPcKh7w2JmiPYXIXZMZmU4HEFY130_provenance.
- NP827878.RAtVGwxqCiSW_L_W11HhPcKh7w2JmiPYXIXZMZmU4HEFY130_assertion wasDerivedFrom befree-20140225 NP827878.RAtVGwxqCiSW_L_W11HhPcKh7w2JmiPYXIXZMZmU4HEFY130_provenance.
- NP827878.RAtVGwxqCiSW_L_W11HhPcKh7w2JmiPYXIXZMZmU4HEFY130_assertion wasGeneratedBy ECO_0000203 NP827878.RAtVGwxqCiSW_L_W11HhPcKh7w2JmiPYXIXZMZmU4HEFY130_provenance.
- befree-20140225 importedOn "2014-02-25" NP827878.RAtVGwxqCiSW_L_W11HhPcKh7w2JmiPYXIXZMZmU4HEFY130_provenance.