Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP503032.RAEd1QZcrmVYHUQT1HGzUK9wP3WFM6XmFjLAxHSLBaHDc130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP503032.RAEd1QZcrmVYHUQT1HGzUK9wP3WFM6XmFjLAxHSLBaHDc130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP503032.RAEd1QZcrmVYHUQT1HGzUK9wP3WFM6XmFjLAxHSLBaHDc130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP503032.RAEd1QZcrmVYHUQT1HGzUK9wP3WFM6XmFjLAxHSLBaHDc130_provenance.
- NP503032.RAEd1QZcrmVYHUQT1HGzUK9wP3WFM6XmFjLAxHSLBaHDc130_assertion description "[However, HFE mutations were seen twice as often among carriers of a common BRCA2 mutation 9346(-2)A-->G compared with the rest of the MBC cases, indicating that HFE may be an MBC risk modifier gene among BRCA2 mutation carriers.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP503032.RAEd1QZcrmVYHUQT1HGzUK9wP3WFM6XmFjLAxHSLBaHDc130_provenance.
- NP503032.RAEd1QZcrmVYHUQT1HGzUK9wP3WFM6XmFjLAxHSLBaHDc130_assertion evidence source_evidence_literature NP503032.RAEd1QZcrmVYHUQT1HGzUK9wP3WFM6XmFjLAxHSLBaHDc130_provenance.
- NP503032.RAEd1QZcrmVYHUQT1HGzUK9wP3WFM6XmFjLAxHSLBaHDc130_assertion SIO_000772 16003728 NP503032.RAEd1QZcrmVYHUQT1HGzUK9wP3WFM6XmFjLAxHSLBaHDc130_provenance.
- NP503032.RAEd1QZcrmVYHUQT1HGzUK9wP3WFM6XmFjLAxHSLBaHDc130_assertion wasDerivedFrom befree-2016 NP503032.RAEd1QZcrmVYHUQT1HGzUK9wP3WFM6XmFjLAxHSLBaHDc130_provenance.
- NP503032.RAEd1QZcrmVYHUQT1HGzUK9wP3WFM6XmFjLAxHSLBaHDc130_assertion wasGeneratedBy ECO_0000203 NP503032.RAEd1QZcrmVYHUQT1HGzUK9wP3WFM6XmFjLAxHSLBaHDc130_provenance.
- befree-2016 importedOn "2016-02-19" NP503032.RAEd1QZcrmVYHUQT1HGzUK9wP3WFM6XmFjLAxHSLBaHDc130_provenance.