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- source_evidence_literature type ECO_0000212 NP978219.RAH-RfUMm_V4BTSuc27xnll4NxeLfD5XeS1GeJOX0dbuE130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP978219.RAH-RfUMm_V4BTSuc27xnll4NxeLfD5XeS1GeJOX0dbuE130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP978219.RAH-RfUMm_V4BTSuc27xnll4NxeLfD5XeS1GeJOX0dbuE130_provenance.
- NP978219.RAH-RfUMm_V4BTSuc27xnll4NxeLfD5XeS1GeJOX0dbuE130_assertion description "[We progressively screened DNA samples from 613 individuals with ID initially for the most frequent ARX mutations (c.304ins(GCG)(7)'expansion' of pA1 and c.429_452dup 'dup24bp' of pA2).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP978219.RAH-RfUMm_V4BTSuc27xnll4NxeLfD5XeS1GeJOX0dbuE130_provenance.
- NP978219.RAH-RfUMm_V4BTSuc27xnll4NxeLfD5XeS1GeJOX0dbuE130_assertion evidence source_evidence_literature NP978219.RAH-RfUMm_V4BTSuc27xnll4NxeLfD5XeS1GeJOX0dbuE130_provenance.
- NP978219.RAH-RfUMm_V4BTSuc27xnll4NxeLfD5XeS1GeJOX0dbuE130_assertion SIO_000772 21496008 NP978219.RAH-RfUMm_V4BTSuc27xnll4NxeLfD5XeS1GeJOX0dbuE130_provenance.
- NP978219.RAH-RfUMm_V4BTSuc27xnll4NxeLfD5XeS1GeJOX0dbuE130_assertion wasDerivedFrom befree-20150227 NP978219.RAH-RfUMm_V4BTSuc27xnll4NxeLfD5XeS1GeJOX0dbuE130_provenance.
- NP978219.RAH-RfUMm_V4BTSuc27xnll4NxeLfD5XeS1GeJOX0dbuE130_assertion wasGeneratedBy ECO_0000203 NP978219.RAH-RfUMm_V4BTSuc27xnll4NxeLfD5XeS1GeJOX0dbuE130_provenance.
- befree-20150227 importedOn "2015-02-27" NP978219.RAH-RfUMm_V4BTSuc27xnll4NxeLfD5XeS1GeJOX0dbuE130_provenance.