Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP92422.RANZM3aCu0oXKIAiXJVJrPdHU23ez578S6AcJ0pNdqaLg130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP92422.RANZM3aCu0oXKIAiXJVJrPdHU23ez578S6AcJ0pNdqaLg130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP92422.RANZM3aCu0oXKIAiXJVJrPdHU23ez578S6AcJ0pNdqaLg130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP92422.RANZM3aCu0oXKIAiXJVJrPdHU23ez578S6AcJ0pNdqaLg130_provenance.
- NP92422.RANZM3aCu0oXKIAiXJVJrPdHU23ez578S6AcJ0pNdqaLg130_assertion description "[At MRE11, we observed a significant haplotype association (P(corr) = 0.012), and at RAD51, one common haplotype was significantly associated with ovarian cancer risk (P(corr) = 0.026).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP92422.RANZM3aCu0oXKIAiXJVJrPdHU23ez578S6AcJ0pNdqaLg130_provenance.
- NP92422.RANZM3aCu0oXKIAiXJVJrPdHU23ez578S6AcJ0pNdqaLg130_assertion evidence source_evidence_literature NP92422.RANZM3aCu0oXKIAiXJVJrPdHU23ez578S6AcJ0pNdqaLg130_provenance.
- NP92422.RANZM3aCu0oXKIAiXJVJrPdHU23ez578S6AcJ0pNdqaLg130_assertion SIO_000772 19584272 NP92422.RANZM3aCu0oXKIAiXJVJrPdHU23ez578S6AcJ0pNdqaLg130_provenance.
- NP92422.RANZM3aCu0oXKIAiXJVJrPdHU23ez578S6AcJ0pNdqaLg130_assertion wasDerivedFrom gad-20150221 NP92422.RANZM3aCu0oXKIAiXJVJrPdHU23ez578S6AcJ0pNdqaLg130_provenance.
- NP92422.RANZM3aCu0oXKIAiXJVJrPdHU23ez578S6AcJ0pNdqaLg130_assertion wasGeneratedBy ECO_0000203 NP92422.RANZM3aCu0oXKIAiXJVJrPdHU23ez578S6AcJ0pNdqaLg130_provenance.
- gad-20150221 importedOn "2015-02-21" NP92422.RANZM3aCu0oXKIAiXJVJrPdHU23ez578S6AcJ0pNdqaLg130_provenance.