Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP503405.RAeAmQ5Al3YGc3ltW7Q8YtzqjIvPvHnoxqnv7HOqmG5D0130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP503405.RAeAmQ5Al3YGc3ltW7Q8YtzqjIvPvHnoxqnv7HOqmG5D0130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP503405.RAeAmQ5Al3YGc3ltW7Q8YtzqjIvPvHnoxqnv7HOqmG5D0130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP503405.RAeAmQ5Al3YGc3ltW7Q8YtzqjIvPvHnoxqnv7HOqmG5D0130_provenance.
- NP503405.RAeAmQ5Al3YGc3ltW7Q8YtzqjIvPvHnoxqnv7HOqmG5D0130_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." NP503405.RAeAmQ5Al3YGc3ltW7Q8YtzqjIvPvHnoxqnv7HOqmG5D0130_provenance.
- NP503405.RAeAmQ5Al3YGc3ltW7Q8YtzqjIvPvHnoxqnv7HOqmG5D0130_assertion evidence source_evidence_literature NP503405.RAeAmQ5Al3YGc3ltW7Q8YtzqjIvPvHnoxqnv7HOqmG5D0130_provenance.
- NP503405.RAeAmQ5Al3YGc3ltW7Q8YtzqjIvPvHnoxqnv7HOqmG5D0130_assertion SIO_000772 18662591 NP503405.RAeAmQ5Al3YGc3ltW7Q8YtzqjIvPvHnoxqnv7HOqmG5D0130_provenance.
- NP503405.RAeAmQ5Al3YGc3ltW7Q8YtzqjIvPvHnoxqnv7HOqmG5D0130_assertion wasDerivedFrom befree-20140225 NP503405.RAeAmQ5Al3YGc3ltW7Q8YtzqjIvPvHnoxqnv7HOqmG5D0130_provenance.
- NP503405.RAeAmQ5Al3YGc3ltW7Q8YtzqjIvPvHnoxqnv7HOqmG5D0130_assertion wasGeneratedBy ECO_0000203 NP503405.RAeAmQ5Al3YGc3ltW7Q8YtzqjIvPvHnoxqnv7HOqmG5D0130_provenance.
- befree-20140225 importedOn "2014-02-25" NP503405.RAeAmQ5Al3YGc3ltW7Q8YtzqjIvPvHnoxqnv7HOqmG5D0130_provenance.