Matches in Nanopublications for { ?s ?p "[Our studies suggest that mutations in PDGFRB are a cause of IM and highlight NOTCH3 as a candidate gene.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine."@en ?g. }
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- NP177793.RA7564V9x0Xq0o8yX0ieklnhW4FYc3rFYQXzGqQEYmj3I130_assertion description "[Our studies suggest that mutations in PDGFRB are a cause of IM and highlight NOTCH3 as a candidate gene.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP177793.RA7564V9x0Xq0o8yX0ieklnhW4FYc3rFYQXzGqQEYmj3I130_provenance.
- NP668527.RAmDYV319Vtw1AF2joxuapqNiEfdvSQGR6Zb17ErYYwX8130_assertion description "[Our studies suggest that mutations in PDGFRB are a cause of IM and highlight NOTCH3 as a candidate gene.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP668527.RAmDYV319Vtw1AF2joxuapqNiEfdvSQGR6Zb17ErYYwX8130_provenance.
- NP556049.RAJbA7aODU0WMe9azUhezNxcE3DcT4vdvp6HvOyDDBKfQ130_assertion description "[Our studies suggest that mutations in PDGFRB are a cause of IM and highlight NOTCH3 as a candidate gene.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP556049.RAJbA7aODU0WMe9azUhezNxcE3DcT4vdvp6HvOyDDBKfQ130_provenance.
- assertion description "[Our studies suggest that mutations in PDGFRB are a cause of IM and highlight NOTCH3 as a candidate gene.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." provenance.
- assertion description "[Our studies suggest that mutations in PDGFRB are a cause of IM and highlight NOTCH3 as a candidate gene.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." provenance.
- NP1083008.RAhUO435UBaZR5EV2xSNUAC9e6W2aLZOOpVlpiAnOYHPA130_assertion description "[Our studies suggest that mutations in PDGFRB are a cause of IM and highlight NOTCH3 as a candidate gene.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1083008.RAhUO435UBaZR5EV2xSNUAC9e6W2aLZOOpVlpiAnOYHPA130_provenance.
- NP596535.RA5COY7zBajn__nuBX6p1jCP0zr28baAYg7prMwOXUXXM130_assertion description "[Our studies suggest that mutations in PDGFRB are a cause of IM and highlight NOTCH3 as a candidate gene.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP596535.RA5COY7zBajn__nuBX6p1jCP0zr28baAYg7prMwOXUXXM130_provenance.