Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP616288.RAvLSX9hRHoaufLTSQ1C4fbALEw7LUur5s2OjtGYcXTNI130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP616288.RAvLSX9hRHoaufLTSQ1C4fbALEw7LUur5s2OjtGYcXTNI130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP616288.RAvLSX9hRHoaufLTSQ1C4fbALEw7LUur5s2OjtGYcXTNI130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP616288.RAvLSX9hRHoaufLTSQ1C4fbALEw7LUur5s2OjtGYcXTNI130_provenance.
- NP616288.RAvLSX9hRHoaufLTSQ1C4fbALEw7LUur5s2OjtGYcXTNI130_assertion description "[Only two autosomal genes, the PRSS12 gene on chromosome 4q26 and the CRBN on chromosome 3p26, have been shown to cause autosomal recessive NSMR, each gene in only one family.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP616288.RAvLSX9hRHoaufLTSQ1C4fbALEw7LUur5s2OjtGYcXTNI130_provenance.
- NP616288.RAvLSX9hRHoaufLTSQ1C4fbALEw7LUur5s2OjtGYcXTNI130_assertion evidence source_evidence_literature NP616288.RAvLSX9hRHoaufLTSQ1C4fbALEw7LUur5s2OjtGYcXTNI130_provenance.
- NP616288.RAvLSX9hRHoaufLTSQ1C4fbALEw7LUur5s2OjtGYcXTNI130_assertion SIO_000772 16033914 NP616288.RAvLSX9hRHoaufLTSQ1C4fbALEw7LUur5s2OjtGYcXTNI130_provenance.
- NP616288.RAvLSX9hRHoaufLTSQ1C4fbALEw7LUur5s2OjtGYcXTNI130_assertion wasDerivedFrom befree-20140225 NP616288.RAvLSX9hRHoaufLTSQ1C4fbALEw7LUur5s2OjtGYcXTNI130_provenance.
- NP616288.RAvLSX9hRHoaufLTSQ1C4fbALEw7LUur5s2OjtGYcXTNI130_assertion wasGeneratedBy ECO_0000203 NP616288.RAvLSX9hRHoaufLTSQ1C4fbALEw7LUur5s2OjtGYcXTNI130_provenance.
- befree-20140225 importedOn "2014-02-25" NP616288.RAvLSX9hRHoaufLTSQ1C4fbALEw7LUur5s2OjtGYcXTNI130_provenance.