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- source_evidence_literature type ECO_0000212 NP597439.RAAJumsEhad0-FomxKrbSrTrPk9jXZqvLe3mxLGtBQcb4130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP597439.RAAJumsEhad0-FomxKrbSrTrPk9jXZqvLe3mxLGtBQcb4130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP597439.RAAJumsEhad0-FomxKrbSrTrPk9jXZqvLe3mxLGtBQcb4130_provenance.
- NP597439.RAAJumsEhad0-FomxKrbSrTrPk9jXZqvLe3mxLGtBQcb4130_assertion description "[Rare inactivating mutations in BRCA1, BRCA2, ATM, TP53 and CHEK2 confer relative risks for breast cancer between about 2 and more than 10, but more common variants in these genes are generally considered of little or no clinical significance.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP597439.RAAJumsEhad0-FomxKrbSrTrPk9jXZqvLe3mxLGtBQcb4130_provenance.
- NP597439.RAAJumsEhad0-FomxKrbSrTrPk9jXZqvLe3mxLGtBQcb4130_assertion evidence source_evidence_literature NP597439.RAAJumsEhad0-FomxKrbSrTrPk9jXZqvLe3mxLGtBQcb4130_provenance.
- NP597439.RAAJumsEhad0-FomxKrbSrTrPk9jXZqvLe3mxLGtBQcb4130_assertion SIO_000772 17341484 NP597439.RAAJumsEhad0-FomxKrbSrTrPk9jXZqvLe3mxLGtBQcb4130_provenance.
- NP597439.RAAJumsEhad0-FomxKrbSrTrPk9jXZqvLe3mxLGtBQcb4130_assertion wasDerivedFrom befree-2016 NP597439.RAAJumsEhad0-FomxKrbSrTrPk9jXZqvLe3mxLGtBQcb4130_provenance.
- NP597439.RAAJumsEhad0-FomxKrbSrTrPk9jXZqvLe3mxLGtBQcb4130_assertion wasGeneratedBy ECO_0000203 NP597439.RAAJumsEhad0-FomxKrbSrTrPk9jXZqvLe3mxLGtBQcb4130_provenance.
- befree-2016 importedOn "2016-02-19" NP597439.RAAJumsEhad0-FomxKrbSrTrPk9jXZqvLe3mxLGtBQcb4130_provenance.