Matches in Nanopublications for { <http://rdf.disgenet.org/nanopublications.trig#NP166862.RA3HF1DNE7RSNxHEwnXYBOoIyyZn-EI8kuCclw1K7nads130_assertion> ?p ?o ?g. }
Showing items 1 to 6 of
6
with 100 items per page.
- NP166862.RA3HF1DNE7RSNxHEwnXYBOoIyyZn-EI8kuCclw1K7nads130_assertion type Assertion NP166862.RA3HF1DNE7RSNxHEwnXYBOoIyyZn-EI8kuCclw1K7nads130_head.
- 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.