Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP1295767.RAiCJBMzLEi4_7ASaVOovmvOafTzr-Uw-iE5WB_SH8ytw130_assertion> ?p ?o ?g. }
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- NP1295767.RAiCJBMzLEi4_7ASaVOovmvOafTzr-Uw-iE5WB_SH8ytw130_assertion type Assertion NP1295767.RAiCJBMzLEi4_7ASaVOovmvOafTzr-Uw-iE5WB_SH8ytw130_head.
- NP1295767.RAiCJBMzLEi4_7ASaVOovmvOafTzr-Uw-iE5WB_SH8ytw130_assertion description "[Association between the SMN2 gene copy number and clinical characteristics of patients with spinal muscular atrophy with homozygous deletion of exon 7 of the SMN1 gene.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1295767.RAiCJBMzLEi4_7ASaVOovmvOafTzr-Uw-iE5WB_SH8ytw130_provenance.
- NP1295767.RAiCJBMzLEi4_7ASaVOovmvOafTzr-Uw-iE5WB_SH8ytw130_assertion evidence source_evidence_literature NP1295767.RAiCJBMzLEi4_7ASaVOovmvOafTzr-Uw-iE5WB_SH8ytw130_provenance.
- NP1295767.RAiCJBMzLEi4_7ASaVOovmvOafTzr-Uw-iE5WB_SH8ytw130_assertion SIO_000772 26665550 NP1295767.RAiCJBMzLEi4_7ASaVOovmvOafTzr-Uw-iE5WB_SH8ytw130_provenance.
- NP1295767.RAiCJBMzLEi4_7ASaVOovmvOafTzr-Uw-iE5WB_SH8ytw130_assertion wasDerivedFrom befree-2016 NP1295767.RAiCJBMzLEi4_7ASaVOovmvOafTzr-Uw-iE5WB_SH8ytw130_provenance.
- NP1295767.RAiCJBMzLEi4_7ASaVOovmvOafTzr-Uw-iE5WB_SH8ytw130_assertion wasGeneratedBy ECO_0000203 NP1295767.RAiCJBMzLEi4_7ASaVOovmvOafTzr-Uw-iE5WB_SH8ytw130_provenance.