Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP726414.RAsoKbQu1UbBhLG0WoWPZPno7M6DgBYhMABol6Ry0dSuo130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP726414.RAsoKbQu1UbBhLG0WoWPZPno7M6DgBYhMABol6Ry0dSuo130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP726414.RAsoKbQu1UbBhLG0WoWPZPno7M6DgBYhMABol6Ry0dSuo130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP726414.RAsoKbQu1UbBhLG0WoWPZPno7M6DgBYhMABol6Ry0dSuo130_provenance.
- NP726414.RAsoKbQu1UbBhLG0WoWPZPno7M6DgBYhMABol6Ry0dSuo130_assertion description "[Here we report an early-onset severe neurological phenotype in Spg7(-/-) Afg3l2(Emv66/+) mice, characterized by loss of balance, tremor and ataxia.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP726414.RAsoKbQu1UbBhLG0WoWPZPno7M6DgBYhMABol6Ry0dSuo130_provenance.
- NP726414.RAsoKbQu1UbBhLG0WoWPZPno7M6DgBYhMABol6Ry0dSuo130_assertion evidence source_evidence_literature NP726414.RAsoKbQu1UbBhLG0WoWPZPno7M6DgBYhMABol6Ry0dSuo130_provenance.
- NP726414.RAsoKbQu1UbBhLG0WoWPZPno7M6DgBYhMABol6Ry0dSuo130_assertion SIO_000772 19289403 NP726414.RAsoKbQu1UbBhLG0WoWPZPno7M6DgBYhMABol6Ry0dSuo130_provenance.
- NP726414.RAsoKbQu1UbBhLG0WoWPZPno7M6DgBYhMABol6Ry0dSuo130_assertion wasDerivedFrom befree-2016 NP726414.RAsoKbQu1UbBhLG0WoWPZPno7M6DgBYhMABol6Ry0dSuo130_provenance.
- NP726414.RAsoKbQu1UbBhLG0WoWPZPno7M6DgBYhMABol6Ry0dSuo130_assertion wasGeneratedBy ECO_0000203 NP726414.RAsoKbQu1UbBhLG0WoWPZPno7M6DgBYhMABol6Ry0dSuo130_provenance.
- befree-2016 importedOn "2016-02-19" NP726414.RAsoKbQu1UbBhLG0WoWPZPno7M6DgBYhMABol6Ry0dSuo130_provenance.