Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP4915.RA9GLWEieULM8SLys0_4OaDNhoVtRnBGT60g_XCcIjbaY130_assertion> ?p ?o ?g. }
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- NP4915.RA9GLWEieULM8SLys0_4OaDNhoVtRnBGT60g_XCcIjbaY130_assertion type Assertion NP4915.RA9GLWEieULM8SLys0_4OaDNhoVtRnBGT60g_XCcIjbaY130_head.
- NP4915.RA9GLWEieULM8SLys0_4OaDNhoVtRnBGT60g_XCcIjbaY130_assertion wasGeneratedBy ECO_0000218 NP4915.RA9GLWEieULM8SLys0_4OaDNhoVtRnBGT60g_XCcIjbaY130_provenance.
- NP4915.RA9GLWEieULM8SLys0_4OaDNhoVtRnBGT60g_XCcIjbaY130_assertion wasDerivedFrom uniprot-2016 NP4915.RA9GLWEieULM8SLys0_4OaDNhoVtRnBGT60g_XCcIjbaY130_provenance.
- NP4915.RA9GLWEieULM8SLys0_4OaDNhoVtRnBGT60g_XCcIjbaY130_assertion SIO_000772 17347910 NP4915.RA9GLWEieULM8SLys0_4OaDNhoVtRnBGT60g_XCcIjbaY130_provenance.
- NP4915.RA9GLWEieULM8SLys0_4OaDNhoVtRnBGT60g_XCcIjbaY130_assertion evidence source_evidence_curated NP4915.RA9GLWEieULM8SLys0_4OaDNhoVtRnBGT60g_XCcIjbaY130_provenance.
- NP4915.RA9GLWEieULM8SLys0_4OaDNhoVtRnBGT60g_XCcIjbaY130_assertion description "[Diagnosis of families with familial hypercholesterolaemia and/or Apo B-100 defect by means of DNA analysis of LDL-receptor gene mutations.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP4915.RA9GLWEieULM8SLys0_4OaDNhoVtRnBGT60g_XCcIjbaY130_provenance.