Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP701897.RAH6R4HdlPT3VN9zO5lKIz19Esw7mjWIfoyPzTqvdHAmk130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP701897.RAH6R4HdlPT3VN9zO5lKIz19Esw7mjWIfoyPzTqvdHAmk130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP701897.RAH6R4HdlPT3VN9zO5lKIz19Esw7mjWIfoyPzTqvdHAmk130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP701897.RAH6R4HdlPT3VN9zO5lKIz19Esw7mjWIfoyPzTqvdHAmk130_provenance.
- NP701897.RAH6R4HdlPT3VN9zO5lKIz19Esw7mjWIfoyPzTqvdHAmk130_assertion description "[Of the 44 patients, 14 had brain magnetic resonance imaging (12 males, 2 females; mean age 4 years 2 months [SD 4 years 4 months]; five with sex chromosomal disorders [SCD] and nine with autosomal chromosomal disorders [ACD]).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP701897.RAH6R4HdlPT3VN9zO5lKIz19Esw7mjWIfoyPzTqvdHAmk130_provenance.
- NP701897.RAH6R4HdlPT3VN9zO5lKIz19Esw7mjWIfoyPzTqvdHAmk130_assertion evidence source_evidence_literature NP701897.RAH6R4HdlPT3VN9zO5lKIz19Esw7mjWIfoyPzTqvdHAmk130_provenance.
- NP701897.RAH6R4HdlPT3VN9zO5lKIz19Esw7mjWIfoyPzTqvdHAmk130_assertion SIO_000772 14995083 NP701897.RAH6R4HdlPT3VN9zO5lKIz19Esw7mjWIfoyPzTqvdHAmk130_provenance.
- NP701897.RAH6R4HdlPT3VN9zO5lKIz19Esw7mjWIfoyPzTqvdHAmk130_assertion wasDerivedFrom befree-20150227 NP701897.RAH6R4HdlPT3VN9zO5lKIz19Esw7mjWIfoyPzTqvdHAmk130_provenance.
- NP701897.RAH6R4HdlPT3VN9zO5lKIz19Esw7mjWIfoyPzTqvdHAmk130_assertion wasGeneratedBy ECO_0000203 NP701897.RAH6R4HdlPT3VN9zO5lKIz19Esw7mjWIfoyPzTqvdHAmk130_provenance.
- befree-20150227 importedOn "2015-02-27" NP701897.RAH6R4HdlPT3VN9zO5lKIz19Esw7mjWIfoyPzTqvdHAmk130_provenance.