Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP163654.RAXpBNNkHFT-Brsvt5Tuq4jVOIjdEBZXT4S-F9GHVq574130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP163654.RAXpBNNkHFT-Brsvt5Tuq4jVOIjdEBZXT4S-F9GHVq574130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP163654.RAXpBNNkHFT-Brsvt5Tuq4jVOIjdEBZXT4S-F9GHVq574130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP163654.RAXpBNNkHFT-Brsvt5Tuq4jVOIjdEBZXT4S-F9GHVq574130_provenance.
- NP163654.RAXpBNNkHFT-Brsvt5Tuq4jVOIjdEBZXT4S-F9GHVq574130_assertion description "[Neither the VDR C352T nor the MPO G463A genotype had manifested association with the dysplasia and carcinoma of the disease, whereas the MTHFR 677TT genotype may be a genetic risk factor for esophageal dysplasia and carcinoma]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP163654.RAXpBNNkHFT-Brsvt5Tuq4jVOIjdEBZXT4S-F9GHVq574130_provenance.
- NP163654.RAXpBNNkHFT-Brsvt5Tuq4jVOIjdEBZXT4S-F9GHVq574130_assertion evidence source_evidence_literature NP163654.RAXpBNNkHFT-Brsvt5Tuq4jVOIjdEBZXT4S-F9GHVq574130_provenance.
- NP163654.RAXpBNNkHFT-Brsvt5Tuq4jVOIjdEBZXT4S-F9GHVq574130_assertion SIO_000772 18662591 NP163654.RAXpBNNkHFT-Brsvt5Tuq4jVOIjdEBZXT4S-F9GHVq574130_provenance.
- NP163654.RAXpBNNkHFT-Brsvt5Tuq4jVOIjdEBZXT4S-F9GHVq574130_assertion wasDerivedFrom lhgdn-20090331 NP163654.RAXpBNNkHFT-Brsvt5Tuq4jVOIjdEBZXT4S-F9GHVq574130_provenance.
- NP163654.RAXpBNNkHFT-Brsvt5Tuq4jVOIjdEBZXT4S-F9GHVq574130_assertion wasGeneratedBy ECO_0000203 NP163654.RAXpBNNkHFT-Brsvt5Tuq4jVOIjdEBZXT4S-F9GHVq574130_provenance.
- lhgdn-20090331 importedOn "2009-03-31" NP163654.RAXpBNNkHFT-Brsvt5Tuq4jVOIjdEBZXT4S-F9GHVq574130_provenance.