Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP344407.RAr068JXPFNU4SaQnEW6kSKbP4gZrgenZ2Eq6oKDd6jKU130_provenance>. }
Showing items 1 to 9 of
9
with 100 items per page.
- source_evidence_literature type ECO_0000212 NP344407.RAr068JXPFNU4SaQnEW6kSKbP4gZrgenZ2Eq6oKDd6jKU130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP344407.RAr068JXPFNU4SaQnEW6kSKbP4gZrgenZ2Eq6oKDd6jKU130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP344407.RAr068JXPFNU4SaQnEW6kSKbP4gZrgenZ2Eq6oKDd6jKU130_provenance.
- NP344407.RAr068JXPFNU4SaQnEW6kSKbP4gZrgenZ2Eq6oKDd6jKU130_assertion description "[Homozygous SMN1 (survival motor neuron) gene deletion causes spinal muscular atrophy, and SMN2 gene deletions are possible risk factors in lower motor neuron disease.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP344407.RAr068JXPFNU4SaQnEW6kSKbP4gZrgenZ2Eq6oKDd6jKU130_provenance.
- NP344407.RAr068JXPFNU4SaQnEW6kSKbP4gZrgenZ2Eq6oKDd6jKU130_assertion evidence source_evidence_literature NP344407.RAr068JXPFNU4SaQnEW6kSKbP4gZrgenZ2Eq6oKDd6jKU130_provenance.
- NP344407.RAr068JXPFNU4SaQnEW6kSKbP4gZrgenZ2Eq6oKDd6jKU130_assertion SIO_000772 11835381 NP344407.RAr068JXPFNU4SaQnEW6kSKbP4gZrgenZ2Eq6oKDd6jKU130_provenance.
- NP344407.RAr068JXPFNU4SaQnEW6kSKbP4gZrgenZ2Eq6oKDd6jKU130_assertion wasDerivedFrom befree-2016 NP344407.RAr068JXPFNU4SaQnEW6kSKbP4gZrgenZ2Eq6oKDd6jKU130_provenance.
- NP344407.RAr068JXPFNU4SaQnEW6kSKbP4gZrgenZ2Eq6oKDd6jKU130_assertion wasGeneratedBy ECO_0000203 NP344407.RAr068JXPFNU4SaQnEW6kSKbP4gZrgenZ2Eq6oKDd6jKU130_provenance.
- befree-2016 importedOn "2016-02-19" NP344407.RAr068JXPFNU4SaQnEW6kSKbP4gZrgenZ2Eq6oKDd6jKU130_provenance.