Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP954021.RAoxaV0l6ZUeFgJ3N0IzUFpmMIaPTuq1f0-RDvFrlHt8M130_assertion> ?p ?o ?g. }
Showing items 1 to 6 of
6
with 100 items per page.
- NP954021.RAoxaV0l6ZUeFgJ3N0IzUFpmMIaPTuq1f0-RDvFrlHt8M130_assertion type Assertion NP954021.RAoxaV0l6ZUeFgJ3N0IzUFpmMIaPTuq1f0-RDvFrlHt8M130_head.
- NP954021.RAoxaV0l6ZUeFgJ3N0IzUFpmMIaPTuq1f0-RDvFrlHt8M130_assertion description "[We report five new genes associated with this condition and suggest screening of TFAP2A and FLNA in patients with Peters anomaly and relevant syndromic features and HCCS, NDP and SLC4A11 in patients with isolated Peters anomaly.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP954021.RAoxaV0l6ZUeFgJ3N0IzUFpmMIaPTuq1f0-RDvFrlHt8M130_provenance.
- NP954021.RAoxaV0l6ZUeFgJ3N0IzUFpmMIaPTuq1f0-RDvFrlHt8M130_assertion evidence source_evidence_literature NP954021.RAoxaV0l6ZUeFgJ3N0IzUFpmMIaPTuq1f0-RDvFrlHt8M130_provenance.
- NP954021.RAoxaV0l6ZUeFgJ3N0IzUFpmMIaPTuq1f0-RDvFrlHt8M130_assertion SIO_000772 25182519 NP954021.RAoxaV0l6ZUeFgJ3N0IzUFpmMIaPTuq1f0-RDvFrlHt8M130_provenance.
- NP954021.RAoxaV0l6ZUeFgJ3N0IzUFpmMIaPTuq1f0-RDvFrlHt8M130_assertion wasDerivedFrom befree-20150227 NP954021.RAoxaV0l6ZUeFgJ3N0IzUFpmMIaPTuq1f0-RDvFrlHt8M130_provenance.
- NP954021.RAoxaV0l6ZUeFgJ3N0IzUFpmMIaPTuq1f0-RDvFrlHt8M130_assertion wasGeneratedBy ECO_0000203 NP954021.RAoxaV0l6ZUeFgJ3N0IzUFpmMIaPTuq1f0-RDvFrlHt8M130_provenance.