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- NP596535.RA5COY7zBajn__nuBX6p1jCP0zr28baAYg7prMwOXUXXM130_assertion type Assertion NP596535.RA5COY7zBajn__nuBX6p1jCP0zr28baAYg7prMwOXUXXM130_head.
- 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.
- NP596535.RA5COY7zBajn__nuBX6p1jCP0zr28baAYg7prMwOXUXXM130_assertion evidence source_evidence_literature NP596535.RA5COY7zBajn__nuBX6p1jCP0zr28baAYg7prMwOXUXXM130_provenance.
- NP596535.RA5COY7zBajn__nuBX6p1jCP0zr28baAYg7prMwOXUXXM130_assertion SIO_000772 23731542 NP596535.RA5COY7zBajn__nuBX6p1jCP0zr28baAYg7prMwOXUXXM130_provenance.
- NP596535.RA5COY7zBajn__nuBX6p1jCP0zr28baAYg7prMwOXUXXM130_assertion wasDerivedFrom befree-20150227 NP596535.RA5COY7zBajn__nuBX6p1jCP0zr28baAYg7prMwOXUXXM130_provenance.
- NP596535.RA5COY7zBajn__nuBX6p1jCP0zr28baAYg7prMwOXUXXM130_assertion wasGeneratedBy ECO_0000203 NP596535.RA5COY7zBajn__nuBX6p1jCP0zr28baAYg7prMwOXUXXM130_provenance.