Matches in Nanopublications for { <http://rdf.disgenet.org/nanopublications.trig#NP544635.RAP7294KyoKwT7mO-8CissRAAylpoUp4N5DOXf9j6aStg130_assertion> ?p ?o ?g. }
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- NP544635.RAP7294KyoKwT7mO-8CissRAAylpoUp4N5DOXf9j6aStg130_assertion type Assertion NP544635.RAP7294KyoKwT7mO-8CissRAAylpoUp4N5DOXf9j6aStg130_head.
- NP544635.RAP7294KyoKwT7mO-8CissRAAylpoUp4N5DOXf9j6aStg130_assertion description "[Here, we report two familial cases of LWD with a large Xp terminal deletion (approximately 943 kb) of distal PAR1 encompassing the SHOX gene.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP544635.RAP7294KyoKwT7mO-8CissRAAylpoUp4N5DOXf9j6aStg130_provenance.
- NP544635.RAP7294KyoKwT7mO-8CissRAAylpoUp4N5DOXf9j6aStg130_assertion evidence source_evidence_literature NP544635.RAP7294KyoKwT7mO-8CissRAAylpoUp4N5DOXf9j6aStg130_provenance.
- NP544635.RAP7294KyoKwT7mO-8CissRAAylpoUp4N5DOXf9j6aStg130_assertion SIO_000772 19400538 NP544635.RAP7294KyoKwT7mO-8CissRAAylpoUp4N5DOXf9j6aStg130_provenance.
- NP544635.RAP7294KyoKwT7mO-8CissRAAylpoUp4N5DOXf9j6aStg130_assertion wasDerivedFrom befree-20140225 NP544635.RAP7294KyoKwT7mO-8CissRAAylpoUp4N5DOXf9j6aStg130_provenance.
- NP544635.RAP7294KyoKwT7mO-8CissRAAylpoUp4N5DOXf9j6aStg130_assertion wasGeneratedBy ECO_0000203 NP544635.RAP7294KyoKwT7mO-8CissRAAylpoUp4N5DOXf9j6aStg130_provenance.