Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP173295.RADhxXym2jT_tcUdyPpjSFX3N6D_TKTvsGh7aITQXp6zY130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP173295.RADhxXym2jT_tcUdyPpjSFX3N6D_TKTvsGh7aITQXp6zY130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP173295.RADhxXym2jT_tcUdyPpjSFX3N6D_TKTvsGh7aITQXp6zY130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP173295.RADhxXym2jT_tcUdyPpjSFX3N6D_TKTvsGh7aITQXp6zY130_provenance.
- NP173295.RADhxXym2jT_tcUdyPpjSFX3N6D_TKTvsGh7aITQXp6zY130_assertion description "[Truncating mutations of the RAP80 gene do not seem to be a cause of familial breast cancer/novel RAP80 haplotype or rare missense mutations (p.Ala342Thr, p.Met353Thr and p.Tyr575Asp) may be associated with a modest increased risk of breast cancer.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP173295.RADhxXym2jT_tcUdyPpjSFX3N6D_TKTvsGh7aITQXp6zY130_provenance.
- NP173295.RADhxXym2jT_tcUdyPpjSFX3N6D_TKTvsGh7aITQXp6zY130_assertion evidence source_evidence_literature NP173295.RADhxXym2jT_tcUdyPpjSFX3N6D_TKTvsGh7aITQXp6zY130_provenance.
- NP173295.RADhxXym2jT_tcUdyPpjSFX3N6D_TKTvsGh7aITQXp6zY130_assertion SIO_000772 18306035 NP173295.RADhxXym2jT_tcUdyPpjSFX3N6D_TKTvsGh7aITQXp6zY130_provenance.
- NP173295.RADhxXym2jT_tcUdyPpjSFX3N6D_TKTvsGh7aITQXp6zY130_assertion wasDerivedFrom lhgdn-20090331 NP173295.RADhxXym2jT_tcUdyPpjSFX3N6D_TKTvsGh7aITQXp6zY130_provenance.
- NP173295.RADhxXym2jT_tcUdyPpjSFX3N6D_TKTvsGh7aITQXp6zY130_assertion wasGeneratedBy ECO_0000203 NP173295.RADhxXym2jT_tcUdyPpjSFX3N6D_TKTvsGh7aITQXp6zY130_provenance.
- lhgdn-20090331 importedOn "2009-03-31" NP173295.RADhxXym2jT_tcUdyPpjSFX3N6D_TKTvsGh7aITQXp6zY130_provenance.