Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP648937.RA-iQXY-MK0R3itIFv4d9OQwcvXJ9X5uuHx5TjNkXVyCM130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP648937.RA-iQXY-MK0R3itIFv4d9OQwcvXJ9X5uuHx5TjNkXVyCM130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP648937.RA-iQXY-MK0R3itIFv4d9OQwcvXJ9X5uuHx5TjNkXVyCM130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP648937.RA-iQXY-MK0R3itIFv4d9OQwcvXJ9X5uuHx5TjNkXVyCM130_provenance.
- NP648937.RA-iQXY-MK0R3itIFv4d9OQwcvXJ9X5uuHx5TjNkXVyCM130_assertion description "[In E- and L-selectin, none of the haplotypes was associated with DVT risk.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP648937.RA-iQXY-MK0R3itIFv4d9OQwcvXJ9X5uuHx5TjNkXVyCM130_provenance.
- NP648937.RA-iQXY-MK0R3itIFv4d9OQwcvXJ9X5uuHx5TjNkXVyCM130_assertion evidence source_evidence_literature NP648937.RA-iQXY-MK0R3itIFv4d9OQwcvXJ9X5uuHx5TjNkXVyCM130_provenance.
- NP648937.RA-iQXY-MK0R3itIFv4d9OQwcvXJ9X5uuHx5TjNkXVyCM130_assertion SIO_000772 18182036 NP648937.RA-iQXY-MK0R3itIFv4d9OQwcvXJ9X5uuHx5TjNkXVyCM130_provenance.
- NP648937.RA-iQXY-MK0R3itIFv4d9OQwcvXJ9X5uuHx5TjNkXVyCM130_assertion wasDerivedFrom befree-2016 NP648937.RA-iQXY-MK0R3itIFv4d9OQwcvXJ9X5uuHx5TjNkXVyCM130_provenance.
- NP648937.RA-iQXY-MK0R3itIFv4d9OQwcvXJ9X5uuHx5TjNkXVyCM130_assertion wasGeneratedBy ECO_0000203 NP648937.RA-iQXY-MK0R3itIFv4d9OQwcvXJ9X5uuHx5TjNkXVyCM130_provenance.
- befree-2016 importedOn "2016-02-19" NP648937.RA-iQXY-MK0R3itIFv4d9OQwcvXJ9X5uuHx5TjNkXVyCM130_provenance.