Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP424072.RA2g38fZl5GlNhFMRS9sW_Q7IM4S4Gc4nHL8ILlG3TEVE130_provenance>. }
Showing items 1 to 9 of
9
with 100 items per page.
- source_evidence_literature type ECO_0000212 NP424072.RA2g38fZl5GlNhFMRS9sW_Q7IM4S4Gc4nHL8ILlG3TEVE130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP424072.RA2g38fZl5GlNhFMRS9sW_Q7IM4S4Gc4nHL8ILlG3TEVE130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP424072.RA2g38fZl5GlNhFMRS9sW_Q7IM4S4Gc4nHL8ILlG3TEVE130_provenance.
- NP424072.RA2g38fZl5GlNhFMRS9sW_Q7IM4S4Gc4nHL8ILlG3TEVE130_assertion description "[Except for CCND2, the expressions of all markers were significantly associated with various TGCT subtypes.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP424072.RA2g38fZl5GlNhFMRS9sW_Q7IM4S4Gc4nHL8ILlG3TEVE130_provenance.
- NP424072.RA2g38fZl5GlNhFMRS9sW_Q7IM4S4Gc4nHL8ILlG3TEVE130_assertion evidence source_evidence_literature NP424072.RA2g38fZl5GlNhFMRS9sW_Q7IM4S4Gc4nHL8ILlG3TEVE130_provenance.
- NP424072.RA2g38fZl5GlNhFMRS9sW_Q7IM4S4Gc4nHL8ILlG3TEVE130_assertion SIO_000772 14670177 NP424072.RA2g38fZl5GlNhFMRS9sW_Q7IM4S4Gc4nHL8ILlG3TEVE130_provenance.
- NP424072.RA2g38fZl5GlNhFMRS9sW_Q7IM4S4Gc4nHL8ILlG3TEVE130_assertion wasDerivedFrom befree-2016 NP424072.RA2g38fZl5GlNhFMRS9sW_Q7IM4S4Gc4nHL8ILlG3TEVE130_provenance.
- NP424072.RA2g38fZl5GlNhFMRS9sW_Q7IM4S4Gc4nHL8ILlG3TEVE130_assertion wasGeneratedBy ECO_0000203 NP424072.RA2g38fZl5GlNhFMRS9sW_Q7IM4S4Gc4nHL8ILlG3TEVE130_provenance.
- befree-2016 importedOn "2016-02-19" NP424072.RA2g38fZl5GlNhFMRS9sW_Q7IM4S4Gc4nHL8ILlG3TEVE130_provenance.