Matches in Nanopublications for { <http://rdf.disgenet.org/nanopublications.trig#NP207136.RAWSmb6cpXVRZjWAxIRU7A-1v4uqcL4PsfKDCkWvtQh_0130_assertion> ?p ?o ?g. }
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- NP207136.RAWSmb6cpXVRZjWAxIRU7A-1v4uqcL4PsfKDCkWvtQh_0130_assertion type Assertion NP207136.RAWSmb6cpXVRZjWAxIRU7A-1v4uqcL4PsfKDCkWvtQh_0130_head.
- NP207136.RAWSmb6cpXVRZjWAxIRU7A-1v4uqcL4PsfKDCkWvtQh_0130_assertion description "[In more than 80% of XLI patients the enzyme deficiency is due to large deletions involving the entire STS gene and flanking sequences.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP207136.RAWSmb6cpXVRZjWAxIRU7A-1v4uqcL4PsfKDCkWvtQh_0130_provenance.
- NP207136.RAWSmb6cpXVRZjWAxIRU7A-1v4uqcL4PsfKDCkWvtQh_0130_assertion evidence source_evidence_literature NP207136.RAWSmb6cpXVRZjWAxIRU7A-1v4uqcL4PsfKDCkWvtQh_0130_provenance.
- NP207136.RAWSmb6cpXVRZjWAxIRU7A-1v4uqcL4PsfKDCkWvtQh_0130_assertion SIO_000772 1539590 NP207136.RAWSmb6cpXVRZjWAxIRU7A-1v4uqcL4PsfKDCkWvtQh_0130_provenance.
- NP207136.RAWSmb6cpXVRZjWAxIRU7A-1v4uqcL4PsfKDCkWvtQh_0130_assertion wasDerivedFrom befree-20140225 NP207136.RAWSmb6cpXVRZjWAxIRU7A-1v4uqcL4PsfKDCkWvtQh_0130_provenance.
- NP207136.RAWSmb6cpXVRZjWAxIRU7A-1v4uqcL4PsfKDCkWvtQh_0130_assertion wasGeneratedBy ECO_0000203 NP207136.RAWSmb6cpXVRZjWAxIRU7A-1v4uqcL4PsfKDCkWvtQh_0130_provenance.