Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP198132.RAb3zd2igX1Muydr2kTXunpxBxIKMm2jawD2j_6sEaBmI130_assertion> ?p ?o ?g. }
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- NP198132.RAb3zd2igX1Muydr2kTXunpxBxIKMm2jawD2j_6sEaBmI130_assertion type Assertion NP198132.RAb3zd2igX1Muydr2kTXunpxBxIKMm2jawD2j_6sEaBmI130_head.
- NP198132.RAb3zd2igX1Muydr2kTXunpxBxIKMm2jawD2j_6sEaBmI130_assertion description "[Results describe the characteristic features of myosclerosis myopathy with a homozygous collagen type 6A2 mutation responsible for a peculiar pattern of collagen VI defects.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP198132.RAb3zd2igX1Muydr2kTXunpxBxIKMm2jawD2j_6sEaBmI130_provenance.
- NP198132.RAb3zd2igX1Muydr2kTXunpxBxIKMm2jawD2j_6sEaBmI130_assertion evidence source_evidence_literature NP198132.RAb3zd2igX1Muydr2kTXunpxBxIKMm2jawD2j_6sEaBmI130_provenance.
- NP198132.RAb3zd2igX1Muydr2kTXunpxBxIKMm2jawD2j_6sEaBmI130_assertion SIO_000772 18852439 NP198132.RAb3zd2igX1Muydr2kTXunpxBxIKMm2jawD2j_6sEaBmI130_provenance.
- NP198132.RAb3zd2igX1Muydr2kTXunpxBxIKMm2jawD2j_6sEaBmI130_assertion wasDerivedFrom lhgdn-20090331 NP198132.RAb3zd2igX1Muydr2kTXunpxBxIKMm2jawD2j_6sEaBmI130_provenance.
- NP198132.RAb3zd2igX1Muydr2kTXunpxBxIKMm2jawD2j_6sEaBmI130_assertion wasGeneratedBy ECO_0000203 NP198132.RAb3zd2igX1Muydr2kTXunpxBxIKMm2jawD2j_6sEaBmI130_provenance.