Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP288069.RAhMV-IW38HU6HBNSTAjCd65H0Nn5bHoxUrTC9kJeqJZo130_provenance>. }
Showing items 1 to 9 of
9
with 100 items per page.
- source_evidence_literature type ECO_0000212 NP288069.RAhMV-IW38HU6HBNSTAjCd65H0Nn5bHoxUrTC9kJeqJZo130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP288069.RAhMV-IW38HU6HBNSTAjCd65H0Nn5bHoxUrTC9kJeqJZo130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP288069.RAhMV-IW38HU6HBNSTAjCd65H0Nn5bHoxUrTC9kJeqJZo130_provenance.
- NP288069.RAhMV-IW38HU6HBNSTAjCd65H0Nn5bHoxUrTC9kJeqJZo130_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." NP288069.RAhMV-IW38HU6HBNSTAjCd65H0Nn5bHoxUrTC9kJeqJZo130_provenance.
- NP288069.RAhMV-IW38HU6HBNSTAjCd65H0Nn5bHoxUrTC9kJeqJZo130_assertion evidence source_evidence_literature NP288069.RAhMV-IW38HU6HBNSTAjCd65H0Nn5bHoxUrTC9kJeqJZo130_provenance.
- NP288069.RAhMV-IW38HU6HBNSTAjCd65H0Nn5bHoxUrTC9kJeqJZo130_assertion SIO_000772 14670177 NP288069.RAhMV-IW38HU6HBNSTAjCd65H0Nn5bHoxUrTC9kJeqJZo130_provenance.
- NP288069.RAhMV-IW38HU6HBNSTAjCd65H0Nn5bHoxUrTC9kJeqJZo130_assertion wasDerivedFrom befree-20150227 NP288069.RAhMV-IW38HU6HBNSTAjCd65H0Nn5bHoxUrTC9kJeqJZo130_provenance.
- NP288069.RAhMV-IW38HU6HBNSTAjCd65H0Nn5bHoxUrTC9kJeqJZo130_assertion wasGeneratedBy ECO_0000203 NP288069.RAhMV-IW38HU6HBNSTAjCd65H0Nn5bHoxUrTC9kJeqJZo130_provenance.
- befree-20150227 importedOn "2015-02-27" NP288069.RAhMV-IW38HU6HBNSTAjCd65H0Nn5bHoxUrTC9kJeqJZo130_provenance.