Matches in Nanopublications for { <http://rdf.disgenet.org/nanopublications.trig#NP184680.RAUvqMDwzIasL-ALFXtBaqCS7r2Eq0bgdSq0D4SHZ8I-c130_assertion> ?p ?o ?g. }
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- NP184680.RAUvqMDwzIasL-ALFXtBaqCS7r2Eq0bgdSq0D4SHZ8I-c130_assertion type Assertion NP184680.RAUvqMDwzIasL-ALFXtBaqCS7r2Eq0bgdSq0D4SHZ8I-c130_head.
- NP184680.RAUvqMDwzIasL-ALFXtBaqCS7r2Eq0bgdSq0D4SHZ8I-c130_assertion description "[Here we describe the presence of a SHOX intragenic deletion in a family with LWD, analyzed through different methodologies.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP184680.RAUvqMDwzIasL-ALFXtBaqCS7r2Eq0bgdSq0D4SHZ8I-c130_provenance.
- NP184680.RAUvqMDwzIasL-ALFXtBaqCS7r2Eq0bgdSq0D4SHZ8I-c130_assertion evidence source_evidence_literature NP184680.RAUvqMDwzIasL-ALFXtBaqCS7r2Eq0bgdSq0D4SHZ8I-c130_provenance.
- NP184680.RAUvqMDwzIasL-ALFXtBaqCS7r2Eq0bgdSq0D4SHZ8I-c130_assertion SIO_000772 19169498 NP184680.RAUvqMDwzIasL-ALFXtBaqCS7r2Eq0bgdSq0D4SHZ8I-c130_provenance.
- NP184680.RAUvqMDwzIasL-ALFXtBaqCS7r2Eq0bgdSq0D4SHZ8I-c130_assertion wasDerivedFrom befree-20140225 NP184680.RAUvqMDwzIasL-ALFXtBaqCS7r2Eq0bgdSq0D4SHZ8I-c130_provenance.
- NP184680.RAUvqMDwzIasL-ALFXtBaqCS7r2Eq0bgdSq0D4SHZ8I-c130_assertion wasGeneratedBy ECO_0000203 NP184680.RAUvqMDwzIasL-ALFXtBaqCS7r2Eq0bgdSq0D4SHZ8I-c130_provenance.