Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP245871.RAKdrQgykX6SoeZQqGK43AbHbg4odzzVgIvDvaeko2hec130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP245871.RAKdrQgykX6SoeZQqGK43AbHbg4odzzVgIvDvaeko2hec130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP245871.RAKdrQgykX6SoeZQqGK43AbHbg4odzzVgIvDvaeko2hec130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP245871.RAKdrQgykX6SoeZQqGK43AbHbg4odzzVgIvDvaeko2hec130_provenance.
- NP245871.RAKdrQgykX6SoeZQqGK43AbHbg4odzzVgIvDvaeko2hec130_assertion description "[We have excluded linkage between HMSN I and FY up to theta = 0.15 (lod = -3.01) and also between HMSN I and markers flanking FY; amylase (AMY), polymorphic urinary mucin (PUM), serum amyloid protein (APCS), and alpha-spectrin (SPTA).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP245871.RAKdrQgykX6SoeZQqGK43AbHbg4odzzVgIvDvaeko2hec130_provenance.
- NP245871.RAKdrQgykX6SoeZQqGK43AbHbg4odzzVgIvDvaeko2hec130_assertion evidence source_evidence_literature NP245871.RAKdrQgykX6SoeZQqGK43AbHbg4odzzVgIvDvaeko2hec130_provenance.
- NP245871.RAKdrQgykX6SoeZQqGK43AbHbg4odzzVgIvDvaeko2hec130_assertion SIO_000772 2737679 NP245871.RAKdrQgykX6SoeZQqGK43AbHbg4odzzVgIvDvaeko2hec130_provenance.
- NP245871.RAKdrQgykX6SoeZQqGK43AbHbg4odzzVgIvDvaeko2hec130_assertion wasDerivedFrom befree-20140225 NP245871.RAKdrQgykX6SoeZQqGK43AbHbg4odzzVgIvDvaeko2hec130_provenance.
- NP245871.RAKdrQgykX6SoeZQqGK43AbHbg4odzzVgIvDvaeko2hec130_assertion wasGeneratedBy ECO_0000203 NP245871.RAKdrQgykX6SoeZQqGK43AbHbg4odzzVgIvDvaeko2hec130_provenance.
- befree-20140225 importedOn "2014-02-25" NP245871.RAKdrQgykX6SoeZQqGK43AbHbg4odzzVgIvDvaeko2hec130_provenance.