Matches in Nanopublications for { <http://rdf.disgenet.org/nanopublications.trig#NP639987.RAbaOSnApdmJmp1NEpCx-fYwNxHITp3zvxHq8vzLFV62k130_assertion> ?p ?o ?g. }
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- NP639987.RAbaOSnApdmJmp1NEpCx-fYwNxHITp3zvxHq8vzLFV62k130_assertion type Assertion NP639987.RAbaOSnApdmJmp1NEpCx-fYwNxHITp3zvxHq8vzLFV62k130_head.
- NP639987.RAbaOSnApdmJmp1NEpCx-fYwNxHITp3zvxHq8vzLFV62k130_assertion wasGeneratedBy ECO_0000203 NP639987.RAbaOSnApdmJmp1NEpCx-fYwNxHITp3zvxHq8vzLFV62k130_provenance.
- NP639987.RAbaOSnApdmJmp1NEpCx-fYwNxHITp3zvxHq8vzLFV62k130_assertion wasDerivedFrom befree-20140225 NP639987.RAbaOSnApdmJmp1NEpCx-fYwNxHITp3zvxHq8vzLFV62k130_provenance.
- NP639987.RAbaOSnApdmJmp1NEpCx-fYwNxHITp3zvxHq8vzLFV62k130_assertion SIO_000772 20025960 NP639987.RAbaOSnApdmJmp1NEpCx-fYwNxHITp3zvxHq8vzLFV62k130_provenance.
- NP639987.RAbaOSnApdmJmp1NEpCx-fYwNxHITp3zvxHq8vzLFV62k130_assertion evidence source_evidence_literature NP639987.RAbaOSnApdmJmp1NEpCx-fYwNxHITp3zvxHq8vzLFV62k130_provenance.
- NP639987.RAbaOSnApdmJmp1NEpCx-fYwNxHITp3zvxHq8vzLFV62k130_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 1 (SMN1) gene.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP639987.RAbaOSnApdmJmp1NEpCx-fYwNxHITp3zvxHq8vzLFV62k130_provenance.