Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP1147493.RALvUSW0Woy-0jYwD5FQUAUyySqiEqxp1uKJPQbNY55Qw130_provenance>. }
Showing items 1 to 9 of
9
with 100 items per page.
- source_evidence_literature type ECO_0000212 NP1147493.RALvUSW0Woy-0jYwD5FQUAUyySqiEqxp1uKJPQbNY55Qw130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP1147493.RALvUSW0Woy-0jYwD5FQUAUyySqiEqxp1uKJPQbNY55Qw130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP1147493.RALvUSW0Woy-0jYwD5FQUAUyySqiEqxp1uKJPQbNY55Qw130_provenance.
- NP1147493.RALvUSW0Woy-0jYwD5FQUAUyySqiEqxp1uKJPQbNY55Qw130_assertion description "[Additional molecular genetics alteration, including mutations of CTNNB1, PPP2R1A, and TP53, may contribute to tumor progression from EMC to UC.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1147493.RALvUSW0Woy-0jYwD5FQUAUyySqiEqxp1uKJPQbNY55Qw130_provenance.
- NP1147493.RALvUSW0Woy-0jYwD5FQUAUyySqiEqxp1uKJPQbNY55Qw130_assertion evidence source_evidence_literature NP1147493.RALvUSW0Woy-0jYwD5FQUAUyySqiEqxp1uKJPQbNY55Qw130_provenance.
- NP1147493.RALvUSW0Woy-0jYwD5FQUAUyySqiEqxp1uKJPQbNY55Qw130_assertion SIO_000772 24451280 NP1147493.RALvUSW0Woy-0jYwD5FQUAUyySqiEqxp1uKJPQbNY55Qw130_provenance.
- NP1147493.RALvUSW0Woy-0jYwD5FQUAUyySqiEqxp1uKJPQbNY55Qw130_assertion wasDerivedFrom befree-2016 NP1147493.RALvUSW0Woy-0jYwD5FQUAUyySqiEqxp1uKJPQbNY55Qw130_provenance.
- NP1147493.RALvUSW0Woy-0jYwD5FQUAUyySqiEqxp1uKJPQbNY55Qw130_assertion wasGeneratedBy ECO_0000203 NP1147493.RALvUSW0Woy-0jYwD5FQUAUyySqiEqxp1uKJPQbNY55Qw130_provenance.
- befree-2016 importedOn "2016-02-19" NP1147493.RALvUSW0Woy-0jYwD5FQUAUyySqiEqxp1uKJPQbNY55Qw130_provenance.