Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP908959.RAaVaJLpxzCGg2no4sUczIrEMEcwBpS9C4VbceXOYX760130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP908959.RAaVaJLpxzCGg2no4sUczIrEMEcwBpS9C4VbceXOYX760130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP908959.RAaVaJLpxzCGg2no4sUczIrEMEcwBpS9C4VbceXOYX760130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP908959.RAaVaJLpxzCGg2no4sUczIrEMEcwBpS9C4VbceXOYX760130_provenance.
- 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.
- befree-20140225 importedOn "2014-02-25" NP908959.RAaVaJLpxzCGg2no4sUczIrEMEcwBpS9C4VbceXOYX760130_provenance.