Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP569570.RAhTtzE370MddvCELz8MNMpMoJPZSl91mGgB3qGaM-v8c130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP569570.RAhTtzE370MddvCELz8MNMpMoJPZSl91mGgB3qGaM-v8c130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP569570.RAhTtzE370MddvCELz8MNMpMoJPZSl91mGgB3qGaM-v8c130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP569570.RAhTtzE370MddvCELz8MNMpMoJPZSl91mGgB3qGaM-v8c130_provenance.
- NP569570.RAhTtzE370MddvCELz8MNMpMoJPZSl91mGgB3qGaM-v8c130_assertion description "[The boy manifested, due to nullisomy of this region, short stature (SHOX), chondrodysplasia punctata (ARSE), and mental retardation (putative mental retardation gene MRX 49).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP569570.RAhTtzE370MddvCELz8MNMpMoJPZSl91mGgB3qGaM-v8c130_provenance.
- NP569570.RAhTtzE370MddvCELz8MNMpMoJPZSl91mGgB3qGaM-v8c130_assertion evidence source_evidence_literature NP569570.RAhTtzE370MddvCELz8MNMpMoJPZSl91mGgB3qGaM-v8c130_provenance.
- NP569570.RAhTtzE370MddvCELz8MNMpMoJPZSl91mGgB3qGaM-v8c130_assertion SIO_000772 10232745 NP569570.RAhTtzE370MddvCELz8MNMpMoJPZSl91mGgB3qGaM-v8c130_provenance.
- NP569570.RAhTtzE370MddvCELz8MNMpMoJPZSl91mGgB3qGaM-v8c130_assertion wasDerivedFrom befree-20150227 NP569570.RAhTtzE370MddvCELz8MNMpMoJPZSl91mGgB3qGaM-v8c130_provenance.
- NP569570.RAhTtzE370MddvCELz8MNMpMoJPZSl91mGgB3qGaM-v8c130_assertion wasGeneratedBy ECO_0000203 NP569570.RAhTtzE370MddvCELz8MNMpMoJPZSl91mGgB3qGaM-v8c130_provenance.
- befree-20150227 importedOn "2015-02-27" NP569570.RAhTtzE370MddvCELz8MNMpMoJPZSl91mGgB3qGaM-v8c130_provenance.