Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP1254789.RAMdtG4-VL2hXFaV6M2p3jQPmz3M0UDUyPzQNBTuvymHc130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP1254789.RAMdtG4-VL2hXFaV6M2p3jQPmz3M0UDUyPzQNBTuvymHc130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP1254789.RAMdtG4-VL2hXFaV6M2p3jQPmz3M0UDUyPzQNBTuvymHc130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP1254789.RAMdtG4-VL2hXFaV6M2p3jQPmz3M0UDUyPzQNBTuvymHc130_provenance.
- befree-2016 importedOn "2016-02-19" NP1254789.RAMdtG4-VL2hXFaV6M2p3jQPmz3M0UDUyPzQNBTuvymHc130_provenance.
- NP1254789.RAMdtG4-VL2hXFaV6M2p3jQPmz3M0UDUyPzQNBTuvymHc130_assertion wasGeneratedBy ECO_0000203 NP1254789.RAMdtG4-VL2hXFaV6M2p3jQPmz3M0UDUyPzQNBTuvymHc130_provenance.
- NP1254789.RAMdtG4-VL2hXFaV6M2p3jQPmz3M0UDUyPzQNBTuvymHc130_assertion wasDerivedFrom befree-2016 NP1254789.RAMdtG4-VL2hXFaV6M2p3jQPmz3M0UDUyPzQNBTuvymHc130_provenance.
- NP1254789.RAMdtG4-VL2hXFaV6M2p3jQPmz3M0UDUyPzQNBTuvymHc130_assertion SIO_000772 25581431 NP1254789.RAMdtG4-VL2hXFaV6M2p3jQPmz3M0UDUyPzQNBTuvymHc130_provenance.
- NP1254789.RAMdtG4-VL2hXFaV6M2p3jQPmz3M0UDUyPzQNBTuvymHc130_assertion evidence source_evidence_literature NP1254789.RAMdtG4-VL2hXFaV6M2p3jQPmz3M0UDUyPzQNBTuvymHc130_provenance.
- NP1254789.RAMdtG4-VL2hXFaV6M2p3jQPmz3M0UDUyPzQNBTuvymHc130_assertion description "[The pattern of association at these loci is consistent in BRCA1 and BRCA2 mutation carriers who are at high risk of EOC.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1254789.RAMdtG4-VL2hXFaV6M2p3jQPmz3M0UDUyPzQNBTuvymHc130_provenance.