Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP166862.RA3HF1DNE7RSNxHEwnXYBOoIyyZn-EI8kuCclw1K7nads130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP166862.RA3HF1DNE7RSNxHEwnXYBOoIyyZn-EI8kuCclw1K7nads130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP166862.RA3HF1DNE7RSNxHEwnXYBOoIyyZn-EI8kuCclw1K7nads130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP166862.RA3HF1DNE7RSNxHEwnXYBOoIyyZn-EI8kuCclw1K7nads130_provenance.
- NP166862.RA3HF1DNE7RSNxHEwnXYBOoIyyZn-EI8kuCclw1K7nads130_assertion wasGeneratedBy ECO_0000203 NP166862.RA3HF1DNE7RSNxHEwnXYBOoIyyZn-EI8kuCclw1K7nads130_provenance.
- NP166862.RA3HF1DNE7RSNxHEwnXYBOoIyyZn-EI8kuCclw1K7nads130_assertion wasDerivedFrom befree-20140225 NP166862.RA3HF1DNE7RSNxHEwnXYBOoIyyZn-EI8kuCclw1K7nads130_provenance.
- NP166862.RA3HF1DNE7RSNxHEwnXYBOoIyyZn-EI8kuCclw1K7nads130_assertion SIO_000772 23000143 NP166862.RA3HF1DNE7RSNxHEwnXYBOoIyyZn-EI8kuCclw1K7nads130_provenance.
- NP166862.RA3HF1DNE7RSNxHEwnXYBOoIyyZn-EI8kuCclw1K7nads130_assertion evidence source_evidence_literature NP166862.RA3HF1DNE7RSNxHEwnXYBOoIyyZn-EI8kuCclw1K7nads130_provenance.
- NP166862.RA3HF1DNE7RSNxHEwnXYBOoIyyZn-EI8kuCclw1K7nads130_assertion description "[A noncoding, regulatory mutation implicates HCFC1 in nonsyndromic intellectual disability.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP166862.RA3HF1DNE7RSNxHEwnXYBOoIyyZn-EI8kuCclw1K7nads130_provenance.
- befree-20140225 importedOn "2014-02-25" NP166862.RA3HF1DNE7RSNxHEwnXYBOoIyyZn-EI8kuCclw1K7nads130_provenance.