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- source_evidence_literature type ECO_0000212 NP1327664.RAn7hkGlNvOmfZXQmw5J4f-UWOdoOpd5UDYe3FvV5DTrE130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP1327664.RAn7hkGlNvOmfZXQmw5J4f-UWOdoOpd5UDYe3FvV5DTrE130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP1327664.RAn7hkGlNvOmfZXQmw5J4f-UWOdoOpd5UDYe3FvV5DTrE130_provenance.
- NP1327664.RAn7hkGlNvOmfZXQmw5J4f-UWOdoOpd5UDYe3FvV5DTrE130_assertion description "[Of the remaining three families studied for linkage, one showed lod scores compatible with exclusion of both MSH2 and MLH1, while lod scores obtained in the other two families suggested exclusion of one HNPCC locus (MSH2 or MLH1) but were uninformative for markers flanking the other locus.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1327664.RAn7hkGlNvOmfZXQmw5J4f-UWOdoOpd5UDYe3FvV5DTrE130_provenance.
- NP1327664.RAn7hkGlNvOmfZXQmw5J4f-UWOdoOpd5UDYe3FvV5DTrE130_assertion evidence source_evidence_literature NP1327664.RAn7hkGlNvOmfZXQmw5J4f-UWOdoOpd5UDYe3FvV5DTrE130_provenance.
- NP1327664.RAn7hkGlNvOmfZXQmw5J4f-UWOdoOpd5UDYe3FvV5DTrE130_assertion SIO_000772 7942843 NP1327664.RAn7hkGlNvOmfZXQmw5J4f-UWOdoOpd5UDYe3FvV5DTrE130_provenance.
- NP1327664.RAn7hkGlNvOmfZXQmw5J4f-UWOdoOpd5UDYe3FvV5DTrE130_assertion wasDerivedFrom befree-2016 NP1327664.RAn7hkGlNvOmfZXQmw5J4f-UWOdoOpd5UDYe3FvV5DTrE130_provenance.
- NP1327664.RAn7hkGlNvOmfZXQmw5J4f-UWOdoOpd5UDYe3FvV5DTrE130_assertion wasGeneratedBy ECO_0000203 NP1327664.RAn7hkGlNvOmfZXQmw5J4f-UWOdoOpd5UDYe3FvV5DTrE130_provenance.
- befree-2016 importedOn "2016-02-19" NP1327664.RAn7hkGlNvOmfZXQmw5J4f-UWOdoOpd5UDYe3FvV5DTrE130_provenance.