Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP758570.RAUC10sWjZDVZhStWRML1V8Odd7t_A1CP5qFcYu_XkZNk130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP758570.RAUC10sWjZDVZhStWRML1V8Odd7t_A1CP5qFcYu_XkZNk130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP758570.RAUC10sWjZDVZhStWRML1V8Odd7t_A1CP5qFcYu_XkZNk130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP758570.RAUC10sWjZDVZhStWRML1V8Odd7t_A1CP5qFcYu_XkZNk130_provenance.
- befree-20150227 importedOn "2015-02-27" NP758570.RAUC10sWjZDVZhStWRML1V8Odd7t_A1CP5qFcYu_XkZNk130_provenance.
- NP758570.RAUC10sWjZDVZhStWRML1V8Odd7t_A1CP5qFcYu_XkZNk130_assertion wasGeneratedBy ECO_0000203 NP758570.RAUC10sWjZDVZhStWRML1V8Odd7t_A1CP5qFcYu_XkZNk130_provenance.
- NP758570.RAUC10sWjZDVZhStWRML1V8Odd7t_A1CP5qFcYu_XkZNk130_assertion wasDerivedFrom befree-20150227 NP758570.RAUC10sWjZDVZhStWRML1V8Odd7t_A1CP5qFcYu_XkZNk130_provenance.
- NP758570.RAUC10sWjZDVZhStWRML1V8Odd7t_A1CP5qFcYu_XkZNk130_assertion SIO_000772 17139695 NP758570.RAUC10sWjZDVZhStWRML1V8Odd7t_A1CP5qFcYu_XkZNk130_provenance.
- NP758570.RAUC10sWjZDVZhStWRML1V8Odd7t_A1CP5qFcYu_XkZNk130_assertion evidence source_evidence_literature NP758570.RAUC10sWjZDVZhStWRML1V8Odd7t_A1CP5qFcYu_XkZNk130_provenance.
- NP758570.RAUC10sWjZDVZhStWRML1V8Odd7t_A1CP5qFcYu_XkZNk130_assertion description "[Eleven paternal diseases were discovered, which were Noonan-like syndrome (1), paternal cervical anomalies (1), Goldenhar syndrome (1), dominant autosomal arthrogryposis (1), osteogenesis imperfecta (3), tuberous sclerosis (1), dominant transposition of great vessels (1), Weyers acrofacial dysostosis (1), and autosomal dominant holoprosencephaly (1).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP758570.RAUC10sWjZDVZhStWRML1V8Odd7t_A1CP5qFcYu_XkZNk130_provenance.