Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP264822.RAA0a-pKnOo9ZA1FAX-EgbHIChsY1xH-qJ93jQCsxYImw130_assertion> ?p ?o ?g. }
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- NP264822.RAA0a-pKnOo9ZA1FAX-EgbHIChsY1xH-qJ93jQCsxYImw130_assertion type Assertion NP264822.RAA0a-pKnOo9ZA1FAX-EgbHIChsY1xH-qJ93jQCsxYImw130_head.
- NP264822.RAA0a-pKnOo9ZA1FAX-EgbHIChsY1xH-qJ93jQCsxYImw130_assertion description "[Localization of the gene for autosomal recessive congenital hereditary endothelial dystrophy (CHED2) to chromosome 20 by homozygosity mapping.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP264822.RAA0a-pKnOo9ZA1FAX-EgbHIChsY1xH-qJ93jQCsxYImw130_provenance.
- NP264822.RAA0a-pKnOo9ZA1FAX-EgbHIChsY1xH-qJ93jQCsxYImw130_assertion evidence source_evidence_literature NP264822.RAA0a-pKnOo9ZA1FAX-EgbHIChsY1xH-qJ93jQCsxYImw130_provenance.
- NP264822.RAA0a-pKnOo9ZA1FAX-EgbHIChsY1xH-qJ93jQCsxYImw130_assertion SIO_000772 10512674 NP264822.RAA0a-pKnOo9ZA1FAX-EgbHIChsY1xH-qJ93jQCsxYImw130_provenance.
- NP264822.RAA0a-pKnOo9ZA1FAX-EgbHIChsY1xH-qJ93jQCsxYImw130_assertion wasDerivedFrom befree-2016 NP264822.RAA0a-pKnOo9ZA1FAX-EgbHIChsY1xH-qJ93jQCsxYImw130_provenance.
- NP264822.RAA0a-pKnOo9ZA1FAX-EgbHIChsY1xH-qJ93jQCsxYImw130_assertion wasGeneratedBy ECO_0000203 NP264822.RAA0a-pKnOo9ZA1FAX-EgbHIChsY1xH-qJ93jQCsxYImw130_provenance.