Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP1081291.RA0roieq5GkiubpOGAcKQMnIV6asSAnJE-7adUQGE_lgc130_assertion> ?p ?o ?g. }
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- NP1081291.RA0roieq5GkiubpOGAcKQMnIV6asSAnJE-7adUQGE_lgc130_assertion type Assertion NP1081291.RA0roieq5GkiubpOGAcKQMnIV6asSAnJE-7adUQGE_lgc130_head.
- NP1081291.RA0roieq5GkiubpOGAcKQMnIV6asSAnJE-7adUQGE_lgc130_assertion wasGeneratedBy ECO_0000203 NP1081291.RA0roieq5GkiubpOGAcKQMnIV6asSAnJE-7adUQGE_lgc130_provenance.
- NP1081291.RA0roieq5GkiubpOGAcKQMnIV6asSAnJE-7adUQGE_lgc130_assertion wasDerivedFrom befree-2016 NP1081291.RA0roieq5GkiubpOGAcKQMnIV6asSAnJE-7adUQGE_lgc130_provenance.
- NP1081291.RA0roieq5GkiubpOGAcKQMnIV6asSAnJE-7adUQGE_lgc130_assertion SIO_000772 23714752 NP1081291.RA0roieq5GkiubpOGAcKQMnIV6asSAnJE-7adUQGE_lgc130_provenance.
- NP1081291.RA0roieq5GkiubpOGAcKQMnIV6asSAnJE-7adUQGE_lgc130_assertion evidence source_evidence_literature NP1081291.RA0roieq5GkiubpOGAcKQMnIV6asSAnJE-7adUQGE_lgc130_provenance.
- NP1081291.RA0roieq5GkiubpOGAcKQMnIV6asSAnJE-7adUQGE_lgc130_assertion description "[Whereas mutations in COL4A5 and contiguous X-chromosomal deletions involving COL4A5 and COL4A6 are associated with X-linked Alport syndrome, a nephropathy associated with deafness and cataract, mutations in COL4A6 alone have not been related to any hereditary disease so far.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1081291.RA0roieq5GkiubpOGAcKQMnIV6asSAnJE-7adUQGE_lgc130_provenance.