Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP710150.RA_YSHM4tgFM7ti3ydlC5KsqjSzyPD-mvED_b_B28CJak130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP710150.RA_YSHM4tgFM7ti3ydlC5KsqjSzyPD-mvED_b_B28CJak130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP710150.RA_YSHM4tgFM7ti3ydlC5KsqjSzyPD-mvED_b_B28CJak130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP710150.RA_YSHM4tgFM7ti3ydlC5KsqjSzyPD-mvED_b_B28CJak130_provenance.
- NP710150.RA_YSHM4tgFM7ti3ydlC5KsqjSzyPD-mvED_b_B28CJak130_assertion description "[A clinical, genetic, and biochemical characterization of SPG7 mutations in a large cohort of patients with hereditary spastic paraplegia.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP710150.RA_YSHM4tgFM7ti3ydlC5KsqjSzyPD-mvED_b_B28CJak130_provenance.
- NP710150.RA_YSHM4tgFM7ti3ydlC5KsqjSzyPD-mvED_b_B28CJak130_assertion evidence source_evidence_literature NP710150.RA_YSHM4tgFM7ti3ydlC5KsqjSzyPD-mvED_b_B28CJak130_provenance.
- NP710150.RA_YSHM4tgFM7ti3ydlC5KsqjSzyPD-mvED_b_B28CJak130_assertion SIO_000772 18200586 NP710150.RA_YSHM4tgFM7ti3ydlC5KsqjSzyPD-mvED_b_B28CJak130_provenance.
- NP710150.RA_YSHM4tgFM7ti3ydlC5KsqjSzyPD-mvED_b_B28CJak130_assertion wasDerivedFrom befree-20150227 NP710150.RA_YSHM4tgFM7ti3ydlC5KsqjSzyPD-mvED_b_B28CJak130_provenance.
- NP710150.RA_YSHM4tgFM7ti3ydlC5KsqjSzyPD-mvED_b_B28CJak130_assertion wasGeneratedBy ECO_0000203 NP710150.RA_YSHM4tgFM7ti3ydlC5KsqjSzyPD-mvED_b_B28CJak130_provenance.
- befree-20150227 importedOn "2015-02-27" NP710150.RA_YSHM4tgFM7ti3ydlC5KsqjSzyPD-mvED_b_B28CJak130_provenance.