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- source_evidence_literature type ECO_0000212 NP1295767.RAiCJBMzLEi4_7ASaVOovmvOafTzr-Uw-iE5WB_SH8ytw130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP1295767.RAiCJBMzLEi4_7ASaVOovmvOafTzr-Uw-iE5WB_SH8ytw130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP1295767.RAiCJBMzLEi4_7ASaVOovmvOafTzr-Uw-iE5WB_SH8ytw130_provenance.
- 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.
- befree-2016 importedOn "2016-02-19" NP1295767.RAiCJBMzLEi4_7ASaVOovmvOafTzr-Uw-iE5WB_SH8ytw130_provenance.