Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP673419.RAULhD_W6-WjN9TT0-dvWYTZhCSm4ITfiLyT6CQIoR2XU130_provenance>. }
Showing items 1 to 9 of
9
with 100 items per page.
- source_evidence_literature type ECO_0000212 NP673419.RAULhD_W6-WjN9TT0-dvWYTZhCSm4ITfiLyT6CQIoR2XU130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP673419.RAULhD_W6-WjN9TT0-dvWYTZhCSm4ITfiLyT6CQIoR2XU130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP673419.RAULhD_W6-WjN9TT0-dvWYTZhCSm4ITfiLyT6CQIoR2XU130_provenance.
- NP673419.RAULhD_W6-WjN9TT0-dvWYTZhCSm4ITfiLyT6CQIoR2XU130_assertion description "[Three SNP alleles in BRD2, Cx-36, and ME2 and microdeletions in 15q13.3, 15q11.2, and 16p13.11 also contribute risk to JME.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP673419.RAULhD_W6-WjN9TT0-dvWYTZhCSm4ITfiLyT6CQIoR2XU130_provenance.
- NP673419.RAULhD_W6-WjN9TT0-dvWYTZhCSm4ITfiLyT6CQIoR2XU130_assertion evidence source_evidence_literature NP673419.RAULhD_W6-WjN9TT0-dvWYTZhCSm4ITfiLyT6CQIoR2XU130_provenance.
- NP673419.RAULhD_W6-WjN9TT0-dvWYTZhCSm4ITfiLyT6CQIoR2XU130_assertion SIO_000772 23756480 NP673419.RAULhD_W6-WjN9TT0-dvWYTZhCSm4ITfiLyT6CQIoR2XU130_provenance.
- NP673419.RAULhD_W6-WjN9TT0-dvWYTZhCSm4ITfiLyT6CQIoR2XU130_assertion wasDerivedFrom befree-20150227 NP673419.RAULhD_W6-WjN9TT0-dvWYTZhCSm4ITfiLyT6CQIoR2XU130_provenance.
- NP673419.RAULhD_W6-WjN9TT0-dvWYTZhCSm4ITfiLyT6CQIoR2XU130_assertion wasGeneratedBy ECO_0000203 NP673419.RAULhD_W6-WjN9TT0-dvWYTZhCSm4ITfiLyT6CQIoR2XU130_provenance.
- befree-20150227 importedOn "2015-02-27" NP673419.RAULhD_W6-WjN9TT0-dvWYTZhCSm4ITfiLyT6CQIoR2XU130_provenance.