Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP164569.RAb1PKJfCaz5GIdr2TWhbLb0OGHxf_bVzE4jtvzrDS6ng130_provenance>. }
Showing items 1 to 9 of
9
with 100 items per page.
- source_evidence_literature type ECO_0000212 NP164569.RAb1PKJfCaz5GIdr2TWhbLb0OGHxf_bVzE4jtvzrDS6ng130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP164569.RAb1PKJfCaz5GIdr2TWhbLb0OGHxf_bVzE4jtvzrDS6ng130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP164569.RAb1PKJfCaz5GIdr2TWhbLb0OGHxf_bVzE4jtvzrDS6ng130_provenance.
- NP164569.RAb1PKJfCaz5GIdr2TWhbLb0OGHxf_bVzE4jtvzrDS6ng130_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." NP164569.RAb1PKJfCaz5GIdr2TWhbLb0OGHxf_bVzE4jtvzrDS6ng130_provenance.
- NP164569.RAb1PKJfCaz5GIdr2TWhbLb0OGHxf_bVzE4jtvzrDS6ng130_assertion evidence source_evidence_literature NP164569.RAb1PKJfCaz5GIdr2TWhbLb0OGHxf_bVzE4jtvzrDS6ng130_provenance.
- NP164569.RAb1PKJfCaz5GIdr2TWhbLb0OGHxf_bVzE4jtvzrDS6ng130_assertion SIO_000772 18662591 NP164569.RAb1PKJfCaz5GIdr2TWhbLb0OGHxf_bVzE4jtvzrDS6ng130_provenance.
- NP164569.RAb1PKJfCaz5GIdr2TWhbLb0OGHxf_bVzE4jtvzrDS6ng130_assertion wasDerivedFrom lhgdn-20090331 NP164569.RAb1PKJfCaz5GIdr2TWhbLb0OGHxf_bVzE4jtvzrDS6ng130_provenance.
- NP164569.RAb1PKJfCaz5GIdr2TWhbLb0OGHxf_bVzE4jtvzrDS6ng130_assertion wasGeneratedBy ECO_0000203 NP164569.RAb1PKJfCaz5GIdr2TWhbLb0OGHxf_bVzE4jtvzrDS6ng130_provenance.
- lhgdn-20090331 importedOn "2009-03-31" NP164569.RAb1PKJfCaz5GIdr2TWhbLb0OGHxf_bVzE4jtvzrDS6ng130_provenance.