Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP763145.RAitzOBPm3iV0IoVYcDd1XvkLcyKHcBGxtEWeKEXMQ0xU130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP763145.RAitzOBPm3iV0IoVYcDd1XvkLcyKHcBGxtEWeKEXMQ0xU130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP763145.RAitzOBPm3iV0IoVYcDd1XvkLcyKHcBGxtEWeKEXMQ0xU130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP763145.RAitzOBPm3iV0IoVYcDd1XvkLcyKHcBGxtEWeKEXMQ0xU130_provenance.
- NP763145.RAitzOBPm3iV0IoVYcDd1XvkLcyKHcBGxtEWeKEXMQ0xU130_assertion description "[However, no report correlates the risk of HCC development with mEPHX and XRCC1 haplotypes.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP763145.RAitzOBPm3iV0IoVYcDd1XvkLcyKHcBGxtEWeKEXMQ0xU130_provenance.
- NP763145.RAitzOBPm3iV0IoVYcDd1XvkLcyKHcBGxtEWeKEXMQ0xU130_assertion evidence source_evidence_literature NP763145.RAitzOBPm3iV0IoVYcDd1XvkLcyKHcBGxtEWeKEXMQ0xU130_provenance.
- NP763145.RAitzOBPm3iV0IoVYcDd1XvkLcyKHcBGxtEWeKEXMQ0xU130_assertion SIO_000772 19754350 NP763145.RAitzOBPm3iV0IoVYcDd1XvkLcyKHcBGxtEWeKEXMQ0xU130_provenance.
- NP763145.RAitzOBPm3iV0IoVYcDd1XvkLcyKHcBGxtEWeKEXMQ0xU130_assertion wasDerivedFrom befree-2016 NP763145.RAitzOBPm3iV0IoVYcDd1XvkLcyKHcBGxtEWeKEXMQ0xU130_provenance.
- NP763145.RAitzOBPm3iV0IoVYcDd1XvkLcyKHcBGxtEWeKEXMQ0xU130_assertion wasGeneratedBy ECO_0000203 NP763145.RAitzOBPm3iV0IoVYcDd1XvkLcyKHcBGxtEWeKEXMQ0xU130_provenance.
- befree-2016 importedOn "2016-02-19" NP763145.RAitzOBPm3iV0IoVYcDd1XvkLcyKHcBGxtEWeKEXMQ0xU130_provenance.