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- NP665001.RAFBjhcfHGvYTFWqwEhB8mdNmE9ENPQDi5wg8Ibq8aIhQ130_assertion type Assertion NP665001.RAFBjhcfHGvYTFWqwEhB8mdNmE9ENPQDi5wg8Ibq8aIhQ130_head.
- NP665001.RAFBjhcfHGvYTFWqwEhB8mdNmE9ENPQDi5wg8Ibq8aIhQ130_assertion description "[To investigate whether mutation of a gene in proximity to the chromosome 2 breakpoint underlies the SHFLD, we sought independent evidence of mutations in GLI2, INHBB and two other genes (RALB and FLJ14816) in 44 unrelated patients with SHFM, SHFLD or isolated long bone deficiency.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP665001.RAFBjhcfHGvYTFWqwEhB8mdNmE9ENPQDi5wg8Ibq8aIhQ130_provenance.
- NP665001.RAFBjhcfHGvYTFWqwEhB8mdNmE9ENPQDi5wg8Ibq8aIhQ130_assertion evidence source_evidence_literature NP665001.RAFBjhcfHGvYTFWqwEhB8mdNmE9ENPQDi5wg8Ibq8aIhQ130_provenance.
- NP665001.RAFBjhcfHGvYTFWqwEhB8mdNmE9ENPQDi5wg8Ibq8aIhQ130_assertion SIO_000772 17569090 NP665001.RAFBjhcfHGvYTFWqwEhB8mdNmE9ENPQDi5wg8Ibq8aIhQ130_provenance.
- NP665001.RAFBjhcfHGvYTFWqwEhB8mdNmE9ENPQDi5wg8Ibq8aIhQ130_assertion wasDerivedFrom befree-20150227 NP665001.RAFBjhcfHGvYTFWqwEhB8mdNmE9ENPQDi5wg8Ibq8aIhQ130_provenance.
- NP665001.RAFBjhcfHGvYTFWqwEhB8mdNmE9ENPQDi5wg8Ibq8aIhQ130_assertion wasGeneratedBy ECO_0000203 NP665001.RAFBjhcfHGvYTFWqwEhB8mdNmE9ENPQDi5wg8Ibq8aIhQ130_provenance.