Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP703460.RAYYxvKqHDdY1fr45aCofU3E3Wlr9H5qoBX65NPCuUmFQ130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP703460.RAYYxvKqHDdY1fr45aCofU3E3Wlr9H5qoBX65NPCuUmFQ130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP703460.RAYYxvKqHDdY1fr45aCofU3E3Wlr9H5qoBX65NPCuUmFQ130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP703460.RAYYxvKqHDdY1fr45aCofU3E3Wlr9H5qoBX65NPCuUmFQ130_provenance.
- NP703460.RAYYxvKqHDdY1fr45aCofU3E3Wlr9H5qoBX65NPCuUmFQ130_assertion description "[The disease is characterized by selective loss of spinal cord motor neurons leading to muscle atrophy and is the result of mutations in the survival motor neuron (SMN) gene.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP703460.RAYYxvKqHDdY1fr45aCofU3E3Wlr9H5qoBX65NPCuUmFQ130_provenance.
- NP703460.RAYYxvKqHDdY1fr45aCofU3E3Wlr9H5qoBX65NPCuUmFQ130_assertion evidence source_evidence_literature NP703460.RAYYxvKqHDdY1fr45aCofU3E3Wlr9H5qoBX65NPCuUmFQ130_provenance.
- NP703460.RAYYxvKqHDdY1fr45aCofU3E3Wlr9H5qoBX65NPCuUmFQ130_assertion SIO_000772 16108074 NP703460.RAYYxvKqHDdY1fr45aCofU3E3Wlr9H5qoBX65NPCuUmFQ130_provenance.
- NP703460.RAYYxvKqHDdY1fr45aCofU3E3Wlr9H5qoBX65NPCuUmFQ130_assertion wasDerivedFrom befree-20150227 NP703460.RAYYxvKqHDdY1fr45aCofU3E3Wlr9H5qoBX65NPCuUmFQ130_provenance.
- NP703460.RAYYxvKqHDdY1fr45aCofU3E3Wlr9H5qoBX65NPCuUmFQ130_assertion wasGeneratedBy ECO_0000203 NP703460.RAYYxvKqHDdY1fr45aCofU3E3Wlr9H5qoBX65NPCuUmFQ130_provenance.
- befree-20150227 importedOn "2015-02-27" NP703460.RAYYxvKqHDdY1fr45aCofU3E3Wlr9H5qoBX65NPCuUmFQ130_provenance.