Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP131066.RAA573FyNWZVWb_ih748lN_BLebv8AlhsmrVXJobO4NFc130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP131066.RAA573FyNWZVWb_ih748lN_BLebv8AlhsmrVXJobO4NFc130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP131066.RAA573FyNWZVWb_ih748lN_BLebv8AlhsmrVXJobO4NFc130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP131066.RAA573FyNWZVWb_ih748lN_BLebv8AlhsmrVXJobO4NFc130_provenance.
- NP131066.RAA573FyNWZVWb_ih748lN_BLebv8AlhsmrVXJobO4NFc130_assertion description "[Our data show that loss of function of both hMLH1 and hMSH2 is not involved in sporadic RCC, either by promoter methylation or mutation in their exons.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP131066.RAA573FyNWZVWb_ih748lN_BLebv8AlhsmrVXJobO4NFc130_provenance.
- NP131066.RAA573FyNWZVWb_ih748lN_BLebv8AlhsmrVXJobO4NFc130_assertion evidence source_evidence_literature NP131066.RAA573FyNWZVWb_ih748lN_BLebv8AlhsmrVXJobO4NFc130_provenance.
- NP131066.RAA573FyNWZVWb_ih748lN_BLebv8AlhsmrVXJobO4NFc130_assertion SIO_000772 18325052 NP131066.RAA573FyNWZVWb_ih748lN_BLebv8AlhsmrVXJobO4NFc130_provenance.
- NP131066.RAA573FyNWZVWb_ih748lN_BLebv8AlhsmrVXJobO4NFc130_assertion wasDerivedFrom gad-20150221 NP131066.RAA573FyNWZVWb_ih748lN_BLebv8AlhsmrVXJobO4NFc130_provenance.
- NP131066.RAA573FyNWZVWb_ih748lN_BLebv8AlhsmrVXJobO4NFc130_assertion wasGeneratedBy ECO_0000203 NP131066.RAA573FyNWZVWb_ih748lN_BLebv8AlhsmrVXJobO4NFc130_provenance.
- gad-20150221 importedOn "2015-02-21" NP131066.RAA573FyNWZVWb_ih748lN_BLebv8AlhsmrVXJobO4NFc130_provenance.