Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP478115.RAgh6F78ESWncwUUhShLdibl8mcp0FWuPAJSRgDu0akEg130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP478115.RAgh6F78ESWncwUUhShLdibl8mcp0FWuPAJSRgDu0akEg130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP478115.RAgh6F78ESWncwUUhShLdibl8mcp0FWuPAJSRgDu0akEg130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP478115.RAgh6F78ESWncwUUhShLdibl8mcp0FWuPAJSRgDu0akEg130_provenance.
- NP478115.RAgh6F78ESWncwUUhShLdibl8mcp0FWuPAJSRgDu0akEg130_assertion description "[In the second stage of a two-stage genome screen for susceptibility loci involving 95 families with two or more individuals with autism or related disorders, a maximal multipoint heterogeneity LOD score (HLOD) of 1.96 and a maximal multipoint nonparametric linkage (NPL) score of 2.39 was seen on chromosome 2q.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP478115.RAgh6F78ESWncwUUhShLdibl8mcp0FWuPAJSRgDu0akEg130_provenance.
- NP478115.RAgh6F78ESWncwUUhShLdibl8mcp0FWuPAJSRgDu0akEg130_assertion evidence source_evidence_literature NP478115.RAgh6F78ESWncwUUhShLdibl8mcp0FWuPAJSRgDu0akEg130_provenance.
- NP478115.RAgh6F78ESWncwUUhShLdibl8mcp0FWuPAJSRgDu0akEg130_assertion SIO_000772 11353400 NP478115.RAgh6F78ESWncwUUhShLdibl8mcp0FWuPAJSRgDu0akEg130_provenance.
- NP478115.RAgh6F78ESWncwUUhShLdibl8mcp0FWuPAJSRgDu0akEg130_assertion wasDerivedFrom befree-20140225 NP478115.RAgh6F78ESWncwUUhShLdibl8mcp0FWuPAJSRgDu0akEg130_provenance.
- NP478115.RAgh6F78ESWncwUUhShLdibl8mcp0FWuPAJSRgDu0akEg130_assertion wasGeneratedBy ECO_0000203 NP478115.RAgh6F78ESWncwUUhShLdibl8mcp0FWuPAJSRgDu0akEg130_provenance.
- befree-20140225 importedOn "2014-02-25" NP478115.RAgh6F78ESWncwUUhShLdibl8mcp0FWuPAJSRgDu0akEg130_provenance.