Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP650213.RAjRrMVLIpcysWNaPFBrouiJfo91rDU5COKndyXWMsPDA130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP650213.RAjRrMVLIpcysWNaPFBrouiJfo91rDU5COKndyXWMsPDA130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP650213.RAjRrMVLIpcysWNaPFBrouiJfo91rDU5COKndyXWMsPDA130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP650213.RAjRrMVLIpcysWNaPFBrouiJfo91rDU5COKndyXWMsPDA130_provenance.
- NP650213.RAjRrMVLIpcysWNaPFBrouiJfo91rDU5COKndyXWMsPDA130_assertion description "[The complete clinical phenotype of dup(7)(p15-->pter) includes mental retardation, skull anomalies, large anterior fontanel, cardiovascular defects, joint dislocation and contraction, and gastrointestinal and genital defects.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP650213.RAjRrMVLIpcysWNaPFBrouiJfo91rDU5COKndyXWMsPDA130_provenance.
- NP650213.RAjRrMVLIpcysWNaPFBrouiJfo91rDU5COKndyXWMsPDA130_assertion evidence source_evidence_literature NP650213.RAjRrMVLIpcysWNaPFBrouiJfo91rDU5COKndyXWMsPDA130_provenance.
- NP650213.RAjRrMVLIpcysWNaPFBrouiJfo91rDU5COKndyXWMsPDA130_assertion SIO_000772 8741912 NP650213.RAjRrMVLIpcysWNaPFBrouiJfo91rDU5COKndyXWMsPDA130_provenance.
- NP650213.RAjRrMVLIpcysWNaPFBrouiJfo91rDU5COKndyXWMsPDA130_assertion wasDerivedFrom befree-20140225 NP650213.RAjRrMVLIpcysWNaPFBrouiJfo91rDU5COKndyXWMsPDA130_provenance.
- NP650213.RAjRrMVLIpcysWNaPFBrouiJfo91rDU5COKndyXWMsPDA130_assertion wasGeneratedBy ECO_0000203 NP650213.RAjRrMVLIpcysWNaPFBrouiJfo91rDU5COKndyXWMsPDA130_provenance.
- befree-20140225 importedOn "2014-02-25" NP650213.RAjRrMVLIpcysWNaPFBrouiJfo91rDU5COKndyXWMsPDA130_provenance.