Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP948636.RA1X9j9hzoVrKYiwKNtTXd-_Jmmp0MOliXRRKrkB6xqKA130_provenance>. }
Showing items 1 to 9 of
9
with 100 items per page.
- source_evidence_literature type ECO_0000212 NP948636.RA1X9j9hzoVrKYiwKNtTXd-_Jmmp0MOliXRRKrkB6xqKA130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP948636.RA1X9j9hzoVrKYiwKNtTXd-_Jmmp0MOliXRRKrkB6xqKA130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP948636.RA1X9j9hzoVrKYiwKNtTXd-_Jmmp0MOliXRRKrkB6xqKA130_provenance.
- NP948636.RA1X9j9hzoVrKYiwKNtTXd-_Jmmp0MOliXRRKrkB6xqKA130_assertion description "[MC1R variants increased the risk of sporadic cutaneous melanoma in darker-pigmented Caucasians: a pooled-analysis from the M-SKIP project.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP948636.RA1X9j9hzoVrKYiwKNtTXd-_Jmmp0MOliXRRKrkB6xqKA130_provenance.
- NP948636.RA1X9j9hzoVrKYiwKNtTXd-_Jmmp0MOliXRRKrkB6xqKA130_assertion evidence source_evidence_literature NP948636.RA1X9j9hzoVrKYiwKNtTXd-_Jmmp0MOliXRRKrkB6xqKA130_provenance.
- NP948636.RA1X9j9hzoVrKYiwKNtTXd-_Jmmp0MOliXRRKrkB6xqKA130_assertion SIO_000772 24917043 NP948636.RA1X9j9hzoVrKYiwKNtTXd-_Jmmp0MOliXRRKrkB6xqKA130_provenance.
- NP948636.RA1X9j9hzoVrKYiwKNtTXd-_Jmmp0MOliXRRKrkB6xqKA130_assertion wasDerivedFrom befree-20150227 NP948636.RA1X9j9hzoVrKYiwKNtTXd-_Jmmp0MOliXRRKrkB6xqKA130_provenance.
- NP948636.RA1X9j9hzoVrKYiwKNtTXd-_Jmmp0MOliXRRKrkB6xqKA130_assertion wasGeneratedBy ECO_0000203 NP948636.RA1X9j9hzoVrKYiwKNtTXd-_Jmmp0MOliXRRKrkB6xqKA130_provenance.
- befree-20150227 importedOn "2015-02-27" NP948636.RA1X9j9hzoVrKYiwKNtTXd-_Jmmp0MOliXRRKrkB6xqKA130_provenance.