Matches in Nanopublications for { <http://rdf.disgenet.org/nanopublications.trig#NP134975.RABcd9yh_e9SbvHN3DPIszvdGjDRUwlV-nWo1n0adNNeo130_assertion> ?p ?o ?g. }
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- NP134975.RABcd9yh_e9SbvHN3DPIszvdGjDRUwlV-nWo1n0adNNeo130_assertion type Assertion NP134975.RABcd9yh_e9SbvHN3DPIszvdGjDRUwlV-nWo1n0adNNeo130_head.
- NP134975.RABcd9yh_e9SbvHN3DPIszvdGjDRUwlV-nWo1n0adNNeo130_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." NP134975.RABcd9yh_e9SbvHN3DPIszvdGjDRUwlV-nWo1n0adNNeo130_provenance.
- NP134975.RABcd9yh_e9SbvHN3DPIszvdGjDRUwlV-nWo1n0adNNeo130_assertion evidence source_evidence_literature NP134975.RABcd9yh_e9SbvHN3DPIszvdGjDRUwlV-nWo1n0adNNeo130_provenance.
- NP134975.RABcd9yh_e9SbvHN3DPIszvdGjDRUwlV-nWo1n0adNNeo130_assertion SIO_000772 18852439 NP134975.RABcd9yh_e9SbvHN3DPIszvdGjDRUwlV-nWo1n0adNNeo130_provenance.
- NP134975.RABcd9yh_e9SbvHN3DPIszvdGjDRUwlV-nWo1n0adNNeo130_assertion wasDerivedFrom lhgdn-20090331 NP134975.RABcd9yh_e9SbvHN3DPIszvdGjDRUwlV-nWo1n0adNNeo130_provenance.
- NP134975.RABcd9yh_e9SbvHN3DPIszvdGjDRUwlV-nWo1n0adNNeo130_assertion wasGeneratedBy ECO_0000203 NP134975.RABcd9yh_e9SbvHN3DPIszvdGjDRUwlV-nWo1n0adNNeo130_provenance.