Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP683119.RAhHvYqopTvVSUpCJBo0sHWy2V_7_lmOBHiONXsh3n2Ms130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP683119.RAhHvYqopTvVSUpCJBo0sHWy2V_7_lmOBHiONXsh3n2Ms130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP683119.RAhHvYqopTvVSUpCJBo0sHWy2V_7_lmOBHiONXsh3n2Ms130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP683119.RAhHvYqopTvVSUpCJBo0sHWy2V_7_lmOBHiONXsh3n2Ms130_provenance.
- NP683119.RAhHvYqopTvVSUpCJBo0sHWy2V_7_lmOBHiONXsh3n2Ms130_assertion description "[A novel presenilin 1 mutation (V261L) associated with presenile Alzheimer's disease and spastic paraparesis.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP683119.RAhHvYqopTvVSUpCJBo0sHWy2V_7_lmOBHiONXsh3n2Ms130_provenance.
- NP683119.RAhHvYqopTvVSUpCJBo0sHWy2V_7_lmOBHiONXsh3n2Ms130_assertion evidence source_evidence_literature NP683119.RAhHvYqopTvVSUpCJBo0sHWy2V_7_lmOBHiONXsh3n2Ms130_provenance.
- NP683119.RAhHvYqopTvVSUpCJBo0sHWy2V_7_lmOBHiONXsh3n2Ms130_assertion SIO_000772 18637955 NP683119.RAhHvYqopTvVSUpCJBo0sHWy2V_7_lmOBHiONXsh3n2Ms130_provenance.
- NP683119.RAhHvYqopTvVSUpCJBo0sHWy2V_7_lmOBHiONXsh3n2Ms130_assertion wasDerivedFrom befree-2016 NP683119.RAhHvYqopTvVSUpCJBo0sHWy2V_7_lmOBHiONXsh3n2Ms130_provenance.
- NP683119.RAhHvYqopTvVSUpCJBo0sHWy2V_7_lmOBHiONXsh3n2Ms130_assertion wasGeneratedBy ECO_0000203 NP683119.RAhHvYqopTvVSUpCJBo0sHWy2V_7_lmOBHiONXsh3n2Ms130_provenance.
- befree-2016 importedOn "2016-02-19" NP683119.RAhHvYqopTvVSUpCJBo0sHWy2V_7_lmOBHiONXsh3n2Ms130_provenance.