Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP320028.RAY3SuIaLz7bGz8v_aZomnUFkFadOeQJA0FjHkLdcCF9I130_assertion> ?p ?o ?g. }
Showing items 1 to 6 of
6
with 100 items per page.
- NP320028.RAY3SuIaLz7bGz8v_aZomnUFkFadOeQJA0FjHkLdcCF9I130_assertion type Assertion NP320028.RAY3SuIaLz7bGz8v_aZomnUFkFadOeQJA0FjHkLdcCF9I130_head.
- NP320028.RAY3SuIaLz7bGz8v_aZomnUFkFadOeQJA0FjHkLdcCF9I130_assertion description "[Alport syndrome (ATS) is a type-IV collagen inherited disorder, caused by mutations in COL4A3 and COL4A4 (autosomal recessive) or COL4A5 (X-linked).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP320028.RAY3SuIaLz7bGz8v_aZomnUFkFadOeQJA0FjHkLdcCF9I130_provenance.
- NP320028.RAY3SuIaLz7bGz8v_aZomnUFkFadOeQJA0FjHkLdcCF9I130_assertion evidence source_evidence_literature NP320028.RAY3SuIaLz7bGz8v_aZomnUFkFadOeQJA0FjHkLdcCF9I130_provenance.
- NP320028.RAY3SuIaLz7bGz8v_aZomnUFkFadOeQJA0FjHkLdcCF9I130_assertion SIO_000772 23144074 NP320028.RAY3SuIaLz7bGz8v_aZomnUFkFadOeQJA0FjHkLdcCF9I130_provenance.
- NP320028.RAY3SuIaLz7bGz8v_aZomnUFkFadOeQJA0FjHkLdcCF9I130_assertion wasDerivedFrom befree-20150227 NP320028.RAY3SuIaLz7bGz8v_aZomnUFkFadOeQJA0FjHkLdcCF9I130_provenance.
- NP320028.RAY3SuIaLz7bGz8v_aZomnUFkFadOeQJA0FjHkLdcCF9I130_assertion wasGeneratedBy ECO_0000203 NP320028.RAY3SuIaLz7bGz8v_aZomnUFkFadOeQJA0FjHkLdcCF9I130_provenance.