Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP504651.RAtwwhk_Pb-m06RYGAijAE8F4irjiLVM1YrxikesbI8XQ130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP504651.RAtwwhk_Pb-m06RYGAijAE8F4irjiLVM1YrxikesbI8XQ130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP504651.RAtwwhk_Pb-m06RYGAijAE8F4irjiLVM1YrxikesbI8XQ130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP504651.RAtwwhk_Pb-m06RYGAijAE8F4irjiLVM1YrxikesbI8XQ130_provenance.
- NP504651.RAtwwhk_Pb-m06RYGAijAE8F4irjiLVM1YrxikesbI8XQ130_assertion description "[This is the first report of a patient with partial trisomy 19p13.3 and partial monosomy p36.3.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP504651.RAtwwhk_Pb-m06RYGAijAE8F4irjiLVM1YrxikesbI8XQ130_provenance.
- NP504651.RAtwwhk_Pb-m06RYGAijAE8F4irjiLVM1YrxikesbI8XQ130_assertion evidence source_evidence_literature NP504651.RAtwwhk_Pb-m06RYGAijAE8F4irjiLVM1YrxikesbI8XQ130_provenance.
- NP504651.RAtwwhk_Pb-m06RYGAijAE8F4irjiLVM1YrxikesbI8XQ130_assertion SIO_000772 19610110 NP504651.RAtwwhk_Pb-m06RYGAijAE8F4irjiLVM1YrxikesbI8XQ130_provenance.
- NP504651.RAtwwhk_Pb-m06RYGAijAE8F4irjiLVM1YrxikesbI8XQ130_assertion wasDerivedFrom befree-20140225 NP504651.RAtwwhk_Pb-m06RYGAijAE8F4irjiLVM1YrxikesbI8XQ130_provenance.
- NP504651.RAtwwhk_Pb-m06RYGAijAE8F4irjiLVM1YrxikesbI8XQ130_assertion wasGeneratedBy ECO_0000203 NP504651.RAtwwhk_Pb-m06RYGAijAE8F4irjiLVM1YrxikesbI8XQ130_provenance.
- befree-20140225 importedOn "2014-02-25" NP504651.RAtwwhk_Pb-m06RYGAijAE8F4irjiLVM1YrxikesbI8XQ130_provenance.