Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP705672.RAb7_3YXFTQpKdjDmxLqcx2GIDNP3gUtbtt404_mF1ZRE130_assertion> ?p ?o ?g. }
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- NP705672.RAb7_3YXFTQpKdjDmxLqcx2GIDNP3gUtbtt404_mF1ZRE130_assertion type Assertion NP705672.RAb7_3YXFTQpKdjDmxLqcx2GIDNP3gUtbtt404_mF1ZRE130_head.
- NP705672.RAb7_3YXFTQpKdjDmxLqcx2GIDNP3gUtbtt404_mF1ZRE130_assertion description "[Spinal muscular atrophy (SMA), the leading genetic cause of death in childhood, is an autosomal recessive neuromuscular disorder characterized by progressive muscle weakness, associated with deletions of the survival motor neuron (SMN) gene identified and mapped to chromosome 5q13.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP705672.RAb7_3YXFTQpKdjDmxLqcx2GIDNP3gUtbtt404_mF1ZRE130_provenance.
- NP705672.RAb7_3YXFTQpKdjDmxLqcx2GIDNP3gUtbtt404_mF1ZRE130_assertion evidence source_evidence_literature NP705672.RAb7_3YXFTQpKdjDmxLqcx2GIDNP3gUtbtt404_mF1ZRE130_provenance.
- NP705672.RAb7_3YXFTQpKdjDmxLqcx2GIDNP3gUtbtt404_mF1ZRE130_assertion SIO_000772 19378506 NP705672.RAb7_3YXFTQpKdjDmxLqcx2GIDNP3gUtbtt404_mF1ZRE130_provenance.
- NP705672.RAb7_3YXFTQpKdjDmxLqcx2GIDNP3gUtbtt404_mF1ZRE130_assertion wasDerivedFrom befree-20150227 NP705672.RAb7_3YXFTQpKdjDmxLqcx2GIDNP3gUtbtt404_mF1ZRE130_provenance.
- NP705672.RAb7_3YXFTQpKdjDmxLqcx2GIDNP3gUtbtt404_mF1ZRE130_assertion wasGeneratedBy ECO_0000203 NP705672.RAb7_3YXFTQpKdjDmxLqcx2GIDNP3gUtbtt404_mF1ZRE130_provenance.