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- source_evidence_literature type ECO_0000212 NP1295672.RAYNdBJpu02RKB_t6PCEelQUqczeDGtf1QoXKN3ZpH9Hc130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP1295672.RAYNdBJpu02RKB_t6PCEelQUqczeDGtf1QoXKN3ZpH9Hc130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP1295672.RAYNdBJpu02RKB_t6PCEelQUqczeDGtf1QoXKN3ZpH9Hc130_provenance.
- NP1295672.RAYNdBJpu02RKB_t6PCEelQUqczeDGtf1QoXKN3ZpH9Hc130_assertion description "[The severely affected DMD patients have little or no detectable dystrophin in their muscle, whereas BMD patients have nearly normal concentrations of an altered form of dystrophin; patients with all other neuromuscular diseases have normal dystrophin.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1295672.RAYNdBJpu02RKB_t6PCEelQUqczeDGtf1QoXKN3ZpH9Hc130_provenance.
- NP1295672.RAYNdBJpu02RKB_t6PCEelQUqczeDGtf1QoXKN3ZpH9Hc130_assertion evidence source_evidence_literature NP1295672.RAYNdBJpu02RKB_t6PCEelQUqczeDGtf1QoXKN3ZpH9Hc130_provenance.
- NP1295672.RAYNdBJpu02RKB_t6PCEelQUqczeDGtf1QoXKN3ZpH9Hc130_assertion SIO_000772 2663232 NP1295672.RAYNdBJpu02RKB_t6PCEelQUqczeDGtf1QoXKN3ZpH9Hc130_provenance.
- NP1295672.RAYNdBJpu02RKB_t6PCEelQUqczeDGtf1QoXKN3ZpH9Hc130_assertion wasDerivedFrom befree-2016 NP1295672.RAYNdBJpu02RKB_t6PCEelQUqczeDGtf1QoXKN3ZpH9Hc130_provenance.
- NP1295672.RAYNdBJpu02RKB_t6PCEelQUqczeDGtf1QoXKN3ZpH9Hc130_assertion wasGeneratedBy ECO_0000203 NP1295672.RAYNdBJpu02RKB_t6PCEelQUqczeDGtf1QoXKN3ZpH9Hc130_provenance.
- befree-2016 importedOn "2016-02-19" NP1295672.RAYNdBJpu02RKB_t6PCEelQUqczeDGtf1QoXKN3ZpH9Hc130_provenance.