Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP259686.RAH7j6vKji7c48_0SM_pJ52bHwuyn53HULiLepmKnkzDQ130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP259686.RAH7j6vKji7c48_0SM_pJ52bHwuyn53HULiLepmKnkzDQ130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP259686.RAH7j6vKji7c48_0SM_pJ52bHwuyn53HULiLepmKnkzDQ130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP259686.RAH7j6vKji7c48_0SM_pJ52bHwuyn53HULiLepmKnkzDQ130_provenance.
- NP259686.RAH7j6vKji7c48_0SM_pJ52bHwuyn53HULiLepmKnkzDQ130_assertion description "[The loss of Bax protein expression was not a consequence of Bax frameshift mutations of the G8 tract and could not be attributed to mutations of the p53 coding sequence (exons 5 to 8) which were detected to a similar extent in de novo ALL samples and at relapse.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP259686.RAH7j6vKji7c48_0SM_pJ52bHwuyn53HULiLepmKnkzDQ130_provenance.
- NP259686.RAH7j6vKji7c48_0SM_pJ52bHwuyn53HULiLepmKnkzDQ130_assertion evidence source_evidence_literature NP259686.RAH7j6vKji7c48_0SM_pJ52bHwuyn53HULiLepmKnkzDQ130_provenance.
- NP259686.RAH7j6vKji7c48_0SM_pJ52bHwuyn53HULiLepmKnkzDQ130_assertion SIO_000772 10995007 NP259686.RAH7j6vKji7c48_0SM_pJ52bHwuyn53HULiLepmKnkzDQ130_provenance.
- NP259686.RAH7j6vKji7c48_0SM_pJ52bHwuyn53HULiLepmKnkzDQ130_assertion wasDerivedFrom befree-20150227 NP259686.RAH7j6vKji7c48_0SM_pJ52bHwuyn53HULiLepmKnkzDQ130_provenance.
- NP259686.RAH7j6vKji7c48_0SM_pJ52bHwuyn53HULiLepmKnkzDQ130_assertion wasGeneratedBy ECO_0000203 NP259686.RAH7j6vKji7c48_0SM_pJ52bHwuyn53HULiLepmKnkzDQ130_provenance.
- befree-20150227 importedOn "2015-02-27" NP259686.RAH7j6vKji7c48_0SM_pJ52bHwuyn53HULiLepmKnkzDQ130_provenance.