Matches in Nanopublications for { <http://rdf.disgenet.org/nanopublications.trig#NP908959.RAaVaJLpxzCGg2no4sUczIrEMEcwBpS9C4VbceXOYX760130_assertion> ?p ?o ?g. }
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- NP908959.RAaVaJLpxzCGg2no4sUczIrEMEcwBpS9C4VbceXOYX760130_assertion type Assertion NP908959.RAaVaJLpxzCGg2no4sUczIrEMEcwBpS9C4VbceXOYX760130_head.
- NP908959.RAaVaJLpxzCGg2no4sUczIrEMEcwBpS9C4VbceXOYX760130_assertion description "[Subsequent studies demonstrated that this mutation is present in one-half of all CG1 patients and correlates with the Zellweger syndrome phenotype.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP908959.RAaVaJLpxzCGg2no4sUczIrEMEcwBpS9C4VbceXOYX760130_provenance.
- NP908959.RAaVaJLpxzCGg2no4sUczIrEMEcwBpS9C4VbceXOYX760130_assertion evidence source_evidence_literature NP908959.RAaVaJLpxzCGg2no4sUczIrEMEcwBpS9C4VbceXOYX760130_provenance.
- NP908959.RAaVaJLpxzCGg2no4sUczIrEMEcwBpS9C4VbceXOYX760130_assertion SIO_000772 10447258 NP908959.RAaVaJLpxzCGg2no4sUczIrEMEcwBpS9C4VbceXOYX760130_provenance.
- NP908959.RAaVaJLpxzCGg2no4sUczIrEMEcwBpS9C4VbceXOYX760130_assertion wasDerivedFrom befree-20140225 NP908959.RAaVaJLpxzCGg2no4sUczIrEMEcwBpS9C4VbceXOYX760130_provenance.
- NP908959.RAaVaJLpxzCGg2no4sUczIrEMEcwBpS9C4VbceXOYX760130_assertion wasGeneratedBy ECO_0000203 NP908959.RAaVaJLpxzCGg2no4sUczIrEMEcwBpS9C4VbceXOYX760130_provenance.