Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP312563.RA-XYxcOHPMgraFECGR94Fh0VcaJ2xkXMZsTrJfJjJOAc130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP312563.RA-XYxcOHPMgraFECGR94Fh0VcaJ2xkXMZsTrJfJjJOAc130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP312563.RA-XYxcOHPMgraFECGR94Fh0VcaJ2xkXMZsTrJfJjJOAc130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP312563.RA-XYxcOHPMgraFECGR94Fh0VcaJ2xkXMZsTrJfJjJOAc130_provenance.
- NP312563.RA-XYxcOHPMgraFECGR94Fh0VcaJ2xkXMZsTrJfJjJOAc130_assertion description "[Therefore, such MPZ gene mutations should be searched for in cases of demyelinating neuropathy with acute nerve compression as well as in cases of the HNPP phenotype associated with normal the PMP22 gene.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP312563.RA-XYxcOHPMgraFECGR94Fh0VcaJ2xkXMZsTrJfJjJOAc130_provenance.
- NP312563.RA-XYxcOHPMgraFECGR94Fh0VcaJ2xkXMZsTrJfJjJOAc130_assertion evidence source_evidence_literature NP312563.RA-XYxcOHPMgraFECGR94Fh0VcaJ2xkXMZsTrJfJjJOAc130_provenance.
- NP312563.RA-XYxcOHPMgraFECGR94Fh0VcaJ2xkXMZsTrJfJjJOAc130_assertion SIO_000772 18663734 NP312563.RA-XYxcOHPMgraFECGR94Fh0VcaJ2xkXMZsTrJfJjJOAc130_provenance.
- NP312563.RA-XYxcOHPMgraFECGR94Fh0VcaJ2xkXMZsTrJfJjJOAc130_assertion wasDerivedFrom befree-20140225 NP312563.RA-XYxcOHPMgraFECGR94Fh0VcaJ2xkXMZsTrJfJjJOAc130_provenance.
- NP312563.RA-XYxcOHPMgraFECGR94Fh0VcaJ2xkXMZsTrJfJjJOAc130_assertion wasGeneratedBy ECO_0000203 NP312563.RA-XYxcOHPMgraFECGR94Fh0VcaJ2xkXMZsTrJfJjJOAc130_provenance.
- befree-20140225 importedOn "2014-02-25" NP312563.RA-XYxcOHPMgraFECGR94Fh0VcaJ2xkXMZsTrJfJjJOAc130_provenance.