Matches in Nanopublications for { ?s ?p "[In a second cross-sectional study, 1318 unrelated anonymous samples collected in 2003-2007 from patients with a broad range of signs typically found in neurofibromatosis type 1 (NF1) but no detectable NF1 germline mutation underwent SPRED1 mutation analysis.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine."@en ?g. }
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- NP776357.RARG5WJEtK6WARYglvaA5eHFTfRM4Gjc1fM5d98FjEDbU130_assertion description "[In a second cross-sectional study, 1318 unrelated anonymous samples collected in 2003-2007 from patients with a broad range of signs typically found in neurofibromatosis type 1 (NF1) but no detectable NF1 germline mutation underwent SPRED1 mutation analysis.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP776357.RARG5WJEtK6WARYglvaA5eHFTfRM4Gjc1fM5d98FjEDbU130_provenance.
- assertion description "[In a second cross-sectional study, 1318 unrelated anonymous samples collected in 2003-2007 from patients with a broad range of signs typically found in neurofibromatosis type 1 (NF1) but no detectable NF1 germline mutation underwent SPRED1 mutation analysis.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." provenance.
- NP114757.RAP5shoyJDcHLL2kXhAlUzJYsiW7vHmSvDj7ZlD5J_9kc130_assertion description "[In a second cross-sectional study, 1318 unrelated anonymous samples collected in 2003-2007 from patients with a broad range of signs typically found in neurofibromatosis type 1 (NF1) but no detectable NF1 germline mutation underwent SPRED1 mutation analysis.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP114757.RAP5shoyJDcHLL2kXhAlUzJYsiW7vHmSvDj7ZlD5J_9kc130_provenance.
- NP160257.RAJtHQP_dswdPKwwGzOm--xuIZx84eY4obhjYF4Gz6yC4130_assertion description "[In a second cross-sectional study, 1318 unrelated anonymous samples collected in 2003-2007 from patients with a broad range of signs typically found in neurofibromatosis type 1 (NF1) but no detectable NF1 germline mutation underwent SPRED1 mutation analysis.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP160257.RAJtHQP_dswdPKwwGzOm--xuIZx84eY4obhjYF4Gz6yC4130_provenance.
- NP977301.RAIrij5GcgBuDqe-EgTyAgCqpeN-IBmIMfF4bM6YvdjGY130_assertion description "[In a second cross-sectional study, 1318 unrelated anonymous samples collected in 2003-2007 from patients with a broad range of signs typically found in neurofibromatosis type 1 (NF1) but no detectable NF1 germline mutation underwent SPRED1 mutation analysis.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP977301.RAIrij5GcgBuDqe-EgTyAgCqpeN-IBmIMfF4bM6YvdjGY130_provenance.