Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP257021.RAgS-iSOsDuOJeXIF6Xvy-iLwezZo8QEph9TpE8SwCjFo130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP257021.RAgS-iSOsDuOJeXIF6Xvy-iLwezZo8QEph9TpE8SwCjFo130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP257021.RAgS-iSOsDuOJeXIF6Xvy-iLwezZo8QEph9TpE8SwCjFo130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP257021.RAgS-iSOsDuOJeXIF6Xvy-iLwezZo8QEph9TpE8SwCjFo130_provenance.
- NP257021.RAgS-iSOsDuOJeXIF6Xvy-iLwezZo8QEph9TpE8SwCjFo130_assertion description "[Consistent with published results from similar follow-up studies, we suggest that RAD51C mutations are rare events among high-risk breast cancer and breast/ovarian cancer families.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP257021.RAgS-iSOsDuOJeXIF6Xvy-iLwezZo8QEph9TpE8SwCjFo130_provenance.
- NP257021.RAgS-iSOsDuOJeXIF6Xvy-iLwezZo8QEph9TpE8SwCjFo130_assertion evidence source_evidence_literature NP257021.RAgS-iSOsDuOJeXIF6Xvy-iLwezZo8QEph9TpE8SwCjFo130_provenance.
- NP257021.RAgS-iSOsDuOJeXIF6Xvy-iLwezZo8QEph9TpE8SwCjFo130_assertion SIO_000772 22476429 NP257021.RAgS-iSOsDuOJeXIF6Xvy-iLwezZo8QEph9TpE8SwCjFo130_provenance.
- NP257021.RAgS-iSOsDuOJeXIF6Xvy-iLwezZo8QEph9TpE8SwCjFo130_assertion wasDerivedFrom befree-20140225 NP257021.RAgS-iSOsDuOJeXIF6Xvy-iLwezZo8QEph9TpE8SwCjFo130_provenance.
- NP257021.RAgS-iSOsDuOJeXIF6Xvy-iLwezZo8QEph9TpE8SwCjFo130_assertion wasGeneratedBy ECO_0000203 NP257021.RAgS-iSOsDuOJeXIF6Xvy-iLwezZo8QEph9TpE8SwCjFo130_provenance.
- befree-20140225 importedOn "2014-02-25" NP257021.RAgS-iSOsDuOJeXIF6Xvy-iLwezZo8QEph9TpE8SwCjFo130_provenance.