Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP297516.RA-kWArgZ-nH1Fy3sc1-qNPlWfO-GgPF927nLWE4O9bbo130_provenance>. }
Showing items 1 to 9 of
9
with 100 items per page.
- source_evidence_literature type ECO_0000212 NP297516.RA-kWArgZ-nH1Fy3sc1-qNPlWfO-GgPF927nLWE4O9bbo130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP297516.RA-kWArgZ-nH1Fy3sc1-qNPlWfO-GgPF927nLWE4O9bbo130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP297516.RA-kWArgZ-nH1Fy3sc1-qNPlWfO-GgPF927nLWE4O9bbo130_provenance.
- NP297516.RA-kWArgZ-nH1Fy3sc1-qNPlWfO-GgPF927nLWE4O9bbo130_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 (SMN) gene identified and mapped to chromosome 5q13.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP297516.RA-kWArgZ-nH1Fy3sc1-qNPlWfO-GgPF927nLWE4O9bbo130_provenance.
- NP297516.RA-kWArgZ-nH1Fy3sc1-qNPlWfO-GgPF927nLWE4O9bbo130_assertion evidence source_evidence_literature NP297516.RA-kWArgZ-nH1Fy3sc1-qNPlWfO-GgPF927nLWE4O9bbo130_provenance.
- NP297516.RA-kWArgZ-nH1Fy3sc1-qNPlWfO-GgPF927nLWE4O9bbo130_assertion SIO_000772 19378506 NP297516.RA-kWArgZ-nH1Fy3sc1-qNPlWfO-GgPF927nLWE4O9bbo130_provenance.
- NP297516.RA-kWArgZ-nH1Fy3sc1-qNPlWfO-GgPF927nLWE4O9bbo130_assertion wasDerivedFrom befree-20140225 NP297516.RA-kWArgZ-nH1Fy3sc1-qNPlWfO-GgPF927nLWE4O9bbo130_provenance.
- NP297516.RA-kWArgZ-nH1Fy3sc1-qNPlWfO-GgPF927nLWE4O9bbo130_assertion wasGeneratedBy ECO_0000203 NP297516.RA-kWArgZ-nH1Fy3sc1-qNPlWfO-GgPF927nLWE4O9bbo130_provenance.
- befree-20140225 importedOn "2014-02-25" NP297516.RA-kWArgZ-nH1Fy3sc1-qNPlWfO-GgPF927nLWE4O9bbo130_provenance.