Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP303290.RAw9KvG5EXAed994WcGlF8A0wHovsXz3NxQMDZSPSJoX0130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP303290.RAw9KvG5EXAed994WcGlF8A0wHovsXz3NxQMDZSPSJoX0130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP303290.RAw9KvG5EXAed994WcGlF8A0wHovsXz3NxQMDZSPSJoX0130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP303290.RAw9KvG5EXAed994WcGlF8A0wHovsXz3NxQMDZSPSJoX0130_provenance.
- NP303290.RAw9KvG5EXAed994WcGlF8A0wHovsXz3NxQMDZSPSJoX0130_assertion description "[Since a microsatellite flanking the RXRB gene and two intragenic polymorphisms are associated significantly with WG on chromosome 6p21.3, further investigations should be focussed on extensive fine-mapping in this region by densely mapping with additional markers such as SNPs.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP303290.RAw9KvG5EXAed994WcGlF8A0wHovsXz3NxQMDZSPSJoX0130_provenance.
- NP303290.RAw9KvG5EXAed994WcGlF8A0wHovsXz3NxQMDZSPSJoX0130_assertion evidence source_evidence_literature NP303290.RAw9KvG5EXAed994WcGlF8A0wHovsXz3NxQMDZSPSJoX0130_provenance.
- NP303290.RAw9KvG5EXAed994WcGlF8A0wHovsXz3NxQMDZSPSJoX0130_assertion SIO_000772 16526951 NP303290.RAw9KvG5EXAed994WcGlF8A0wHovsXz3NxQMDZSPSJoX0130_provenance.
- NP303290.RAw9KvG5EXAed994WcGlF8A0wHovsXz3NxQMDZSPSJoX0130_assertion wasDerivedFrom befree-20140225 NP303290.RAw9KvG5EXAed994WcGlF8A0wHovsXz3NxQMDZSPSJoX0130_provenance.
- NP303290.RAw9KvG5EXAed994WcGlF8A0wHovsXz3NxQMDZSPSJoX0130_assertion wasGeneratedBy ECO_0000203 NP303290.RAw9KvG5EXAed994WcGlF8A0wHovsXz3NxQMDZSPSJoX0130_provenance.
- befree-20140225 importedOn "2014-02-25" NP303290.RAw9KvG5EXAed994WcGlF8A0wHovsXz3NxQMDZSPSJoX0130_provenance.