Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP319932.RApK_qyDVUmt3uydCbzuLF4sPFUFzT-c0b2j_gv2Ci3Ho130_assertion> ?p ?o ?g. }
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- NP319932.RApK_qyDVUmt3uydCbzuLF4sPFUFzT-c0b2j_gv2Ci3Ho130_assertion type Assertion NP319932.RApK_qyDVUmt3uydCbzuLF4sPFUFzT-c0b2j_gv2Ci3Ho130_head.
- NP319932.RApK_qyDVUmt3uydCbzuLF4sPFUFzT-c0b2j_gv2Ci3Ho130_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." NP319932.RApK_qyDVUmt3uydCbzuLF4sPFUFzT-c0b2j_gv2Ci3Ho130_provenance.
- NP319932.RApK_qyDVUmt3uydCbzuLF4sPFUFzT-c0b2j_gv2Ci3Ho130_assertion evidence source_evidence_literature NP319932.RApK_qyDVUmt3uydCbzuLF4sPFUFzT-c0b2j_gv2Ci3Ho130_provenance.
- NP319932.RApK_qyDVUmt3uydCbzuLF4sPFUFzT-c0b2j_gv2Ci3Ho130_assertion SIO_000772 23144074 NP319932.RApK_qyDVUmt3uydCbzuLF4sPFUFzT-c0b2j_gv2Ci3Ho130_provenance.
- NP319932.RApK_qyDVUmt3uydCbzuLF4sPFUFzT-c0b2j_gv2Ci3Ho130_assertion wasDerivedFrom befree-20150227 NP319932.RApK_qyDVUmt3uydCbzuLF4sPFUFzT-c0b2j_gv2Ci3Ho130_provenance.
- NP319932.RApK_qyDVUmt3uydCbzuLF4sPFUFzT-c0b2j_gv2Ci3Ho130_assertion wasGeneratedBy ECO_0000203 NP319932.RApK_qyDVUmt3uydCbzuLF4sPFUFzT-c0b2j_gv2Ci3Ho130_provenance.