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- source_evidence_literature type ECO_0000212 NP549843.RAojuB2UA37IZbvTWip__mYwqhHgGW8LBFF9fsmfHxdKk130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP549843.RAojuB2UA37IZbvTWip__mYwqhHgGW8LBFF9fsmfHxdKk130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP549843.RAojuB2UA37IZbvTWip__mYwqhHgGW8LBFF9fsmfHxdKk130_provenance.
- NP549843.RAojuB2UA37IZbvTWip__mYwqhHgGW8LBFF9fsmfHxdKk130_assertion description "[PTEN frequently shows loss of heterozygosity in breast and prostate cancers, and mutations in this gene are responsible for Cowden disease, a rare Mendelian syndrome that includes breast cancer as part of its phenotype.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP549843.RAojuB2UA37IZbvTWip__mYwqhHgGW8LBFF9fsmfHxdKk130_provenance.
- NP549843.RAojuB2UA37IZbvTWip__mYwqhHgGW8LBFF9fsmfHxdKk130_assertion evidence source_evidence_literature NP549843.RAojuB2UA37IZbvTWip__mYwqhHgGW8LBFF9fsmfHxdKk130_provenance.
- NP549843.RAojuB2UA37IZbvTWip__mYwqhHgGW8LBFF9fsmfHxdKk130_assertion SIO_000772 16702386 NP549843.RAojuB2UA37IZbvTWip__mYwqhHgGW8LBFF9fsmfHxdKk130_provenance.
- NP549843.RAojuB2UA37IZbvTWip__mYwqhHgGW8LBFF9fsmfHxdKk130_assertion wasDerivedFrom befree-2016 NP549843.RAojuB2UA37IZbvTWip__mYwqhHgGW8LBFF9fsmfHxdKk130_provenance.
- NP549843.RAojuB2UA37IZbvTWip__mYwqhHgGW8LBFF9fsmfHxdKk130_assertion wasGeneratedBy ECO_0000203 NP549843.RAojuB2UA37IZbvTWip__mYwqhHgGW8LBFF9fsmfHxdKk130_provenance.
- befree-2016 importedOn "2016-02-19" NP549843.RAojuB2UA37IZbvTWip__mYwqhHgGW8LBFF9fsmfHxdKk130_provenance.