Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP783189.RAPzx9I5-MmySGkIpXuJxep0kbKyJj76LuexZG7IaHsN8130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP783189.RAPzx9I5-MmySGkIpXuJxep0kbKyJj76LuexZG7IaHsN8130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP783189.RAPzx9I5-MmySGkIpXuJxep0kbKyJj76LuexZG7IaHsN8130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP783189.RAPzx9I5-MmySGkIpXuJxep0kbKyJj76LuexZG7IaHsN8130_provenance.
- NP783189.RAPzx9I5-MmySGkIpXuJxep0kbKyJj76LuexZG7IaHsN8130_assertion description "[A total of 10 families were studied in which at least two persons in consecutive generations were affected by SAH, a symptomatic IA (SIA) or a presymptomatic IA (PIA).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP783189.RAPzx9I5-MmySGkIpXuJxep0kbKyJj76LuexZG7IaHsN8130_provenance.
- NP783189.RAPzx9I5-MmySGkIpXuJxep0kbKyJj76LuexZG7IaHsN8130_assertion evidence source_evidence_literature NP783189.RAPzx9I5-MmySGkIpXuJxep0kbKyJj76LuexZG7IaHsN8130_provenance.
- NP783189.RAPzx9I5-MmySGkIpXuJxep0kbKyJj76LuexZG7IaHsN8130_assertion SIO_000772 14512962 NP783189.RAPzx9I5-MmySGkIpXuJxep0kbKyJj76LuexZG7IaHsN8130_provenance.
- NP783189.RAPzx9I5-MmySGkIpXuJxep0kbKyJj76LuexZG7IaHsN8130_assertion wasDerivedFrom befree-20140225 NP783189.RAPzx9I5-MmySGkIpXuJxep0kbKyJj76LuexZG7IaHsN8130_provenance.
- NP783189.RAPzx9I5-MmySGkIpXuJxep0kbKyJj76LuexZG7IaHsN8130_assertion wasGeneratedBy ECO_0000203 NP783189.RAPzx9I5-MmySGkIpXuJxep0kbKyJj76LuexZG7IaHsN8130_provenance.
- befree-20140225 importedOn "2014-02-25" NP783189.RAPzx9I5-MmySGkIpXuJxep0kbKyJj76LuexZG7IaHsN8130_provenance.