Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP709958.RAqrY5WDjLs3N_iXwImVW8baXMUxDadV03hwTCuGcOyx0130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP709958.RAqrY5WDjLs3N_iXwImVW8baXMUxDadV03hwTCuGcOyx0130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP709958.RAqrY5WDjLs3N_iXwImVW8baXMUxDadV03hwTCuGcOyx0130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP709958.RAqrY5WDjLs3N_iXwImVW8baXMUxDadV03hwTCuGcOyx0130_provenance.
- NP709958.RAqrY5WDjLs3N_iXwImVW8baXMUxDadV03hwTCuGcOyx0130_assertion description "[Hereditary spastic paraplegia with cerebellar ataxia: a complex phenotype associated with a new SPG4 gene mutation.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP709958.RAqrY5WDjLs3N_iXwImVW8baXMUxDadV03hwTCuGcOyx0130_provenance.
- NP709958.RAqrY5WDjLs3N_iXwImVW8baXMUxDadV03hwTCuGcOyx0130_assertion evidence source_evidence_literature NP709958.RAqrY5WDjLs3N_iXwImVW8baXMUxDadV03hwTCuGcOyx0130_provenance.
- NP709958.RAqrY5WDjLs3N_iXwImVW8baXMUxDadV03hwTCuGcOyx0130_assertion SIO_000772 15667412 NP709958.RAqrY5WDjLs3N_iXwImVW8baXMUxDadV03hwTCuGcOyx0130_provenance.
- NP709958.RAqrY5WDjLs3N_iXwImVW8baXMUxDadV03hwTCuGcOyx0130_assertion wasDerivedFrom befree-20150227 NP709958.RAqrY5WDjLs3N_iXwImVW8baXMUxDadV03hwTCuGcOyx0130_provenance.
- NP709958.RAqrY5WDjLs3N_iXwImVW8baXMUxDadV03hwTCuGcOyx0130_assertion wasGeneratedBy ECO_0000203 NP709958.RAqrY5WDjLs3N_iXwImVW8baXMUxDadV03hwTCuGcOyx0130_provenance.
- befree-20150227 importedOn "2015-02-27" NP709958.RAqrY5WDjLs3N_iXwImVW8baXMUxDadV03hwTCuGcOyx0130_provenance.