Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP750063.RAUHNkwLhbUfjkXErGXZ2NbrCx6khDF3NDrTq6NAL1oWk130_provenance>. }
Showing items 1 to 9 of
9
with 100 items per page.
- source_evidence_literature type ECO_0000212 NP750063.RAUHNkwLhbUfjkXErGXZ2NbrCx6khDF3NDrTq6NAL1oWk130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP750063.RAUHNkwLhbUfjkXErGXZ2NbrCx6khDF3NDrTq6NAL1oWk130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP750063.RAUHNkwLhbUfjkXErGXZ2NbrCx6khDF3NDrTq6NAL1oWk130_provenance.
- NP750063.RAUHNkwLhbUfjkXErGXZ2NbrCx6khDF3NDrTq6NAL1oWk130_assertion description "[Rare high-penetrance factors are expressed in familial clustering of melanoma and include mutations in CDKN2A (encoding p16(INK4a) and p14(ARF)) and CDK4.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP750063.RAUHNkwLhbUfjkXErGXZ2NbrCx6khDF3NDrTq6NAL1oWk130_provenance.
- NP750063.RAUHNkwLhbUfjkXErGXZ2NbrCx6khDF3NDrTq6NAL1oWk130_assertion evidence source_evidence_literature NP750063.RAUHNkwLhbUfjkXErGXZ2NbrCx6khDF3NDrTq6NAL1oWk130_provenance.
- NP750063.RAUHNkwLhbUfjkXErGXZ2NbrCx6khDF3NDrTq6NAL1oWk130_assertion SIO_000772 19585149 NP750063.RAUHNkwLhbUfjkXErGXZ2NbrCx6khDF3NDrTq6NAL1oWk130_provenance.
- NP750063.RAUHNkwLhbUfjkXErGXZ2NbrCx6khDF3NDrTq6NAL1oWk130_assertion wasDerivedFrom befree-2016 NP750063.RAUHNkwLhbUfjkXErGXZ2NbrCx6khDF3NDrTq6NAL1oWk130_provenance.
- NP750063.RAUHNkwLhbUfjkXErGXZ2NbrCx6khDF3NDrTq6NAL1oWk130_assertion wasGeneratedBy ECO_0000203 NP750063.RAUHNkwLhbUfjkXErGXZ2NbrCx6khDF3NDrTq6NAL1oWk130_provenance.
- befree-2016 importedOn "2016-02-19" NP750063.RAUHNkwLhbUfjkXErGXZ2NbrCx6khDF3NDrTq6NAL1oWk130_provenance.