Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP629605.RAE3hyepZmzHoHf6OnPSNQChh1v7sme4Jrgro1hSM2bpA130_assertion> ?p ?o ?g. }
Showing items 1 to 6 of
6
with 100 items per page.
- NP629605.RAE3hyepZmzHoHf6OnPSNQChh1v7sme4Jrgro1hSM2bpA130_assertion type Assertion NP629605.RAE3hyepZmzHoHf6OnPSNQChh1v7sme4Jrgro1hSM2bpA130_head.
- NP629605.RAE3hyepZmzHoHf6OnPSNQChh1v7sme4Jrgro1hSM2bpA130_assertion description "[Cytogenetically invisible microdeletions involving PITX2 in Rieger syndrome.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP629605.RAE3hyepZmzHoHf6OnPSNQChh1v7sme4Jrgro1hSM2bpA130_provenance.
- NP629605.RAE3hyepZmzHoHf6OnPSNQChh1v7sme4Jrgro1hSM2bpA130_assertion evidence source_evidence_literature NP629605.RAE3hyepZmzHoHf6OnPSNQChh1v7sme4Jrgro1hSM2bpA130_provenance.
- NP629605.RAE3hyepZmzHoHf6OnPSNQChh1v7sme4Jrgro1hSM2bpA130_assertion SIO_000772 17850355 NP629605.RAE3hyepZmzHoHf6OnPSNQChh1v7sme4Jrgro1hSM2bpA130_provenance.
- NP629605.RAE3hyepZmzHoHf6OnPSNQChh1v7sme4Jrgro1hSM2bpA130_assertion wasDerivedFrom befree-2016 NP629605.RAE3hyepZmzHoHf6OnPSNQChh1v7sme4Jrgro1hSM2bpA130_provenance.
- NP629605.RAE3hyepZmzHoHf6OnPSNQChh1v7sme4Jrgro1hSM2bpA130_assertion wasGeneratedBy ECO_0000203 NP629605.RAE3hyepZmzHoHf6OnPSNQChh1v7sme4Jrgro1hSM2bpA130_provenance.