Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP441282.RAQLdf-WPWSxsZhMRDIAFkRb9U-mgsOT5LLcq4j2Yh-3w130_provenance>. }
Showing items 1 to 9 of
9
with 100 items per page.
- source_evidence_literature type ECO_0000212 NP441282.RAQLdf-WPWSxsZhMRDIAFkRb9U-mgsOT5LLcq4j2Yh-3w130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP441282.RAQLdf-WPWSxsZhMRDIAFkRb9U-mgsOT5LLcq4j2Yh-3w130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP441282.RAQLdf-WPWSxsZhMRDIAFkRb9U-mgsOT5LLcq4j2Yh-3w130_provenance.
- befree-20150227 importedOn "2015-02-27" NP441282.RAQLdf-WPWSxsZhMRDIAFkRb9U-mgsOT5LLcq4j2Yh-3w130_provenance.
- NP441282.RAQLdf-WPWSxsZhMRDIAFkRb9U-mgsOT5LLcq4j2Yh-3w130_assertion wasGeneratedBy ECO_0000203 NP441282.RAQLdf-WPWSxsZhMRDIAFkRb9U-mgsOT5LLcq4j2Yh-3w130_provenance.
- NP441282.RAQLdf-WPWSxsZhMRDIAFkRb9U-mgsOT5LLcq4j2Yh-3w130_assertion wasDerivedFrom befree-20150227 NP441282.RAQLdf-WPWSxsZhMRDIAFkRb9U-mgsOT5LLcq4j2Yh-3w130_provenance.
- NP441282.RAQLdf-WPWSxsZhMRDIAFkRb9U-mgsOT5LLcq4j2Yh-3w130_assertion SIO_000772 16000562 NP441282.RAQLdf-WPWSxsZhMRDIAFkRb9U-mgsOT5LLcq4j2Yh-3w130_provenance.
- NP441282.RAQLdf-WPWSxsZhMRDIAFkRb9U-mgsOT5LLcq4j2Yh-3w130_assertion evidence source_evidence_literature NP441282.RAQLdf-WPWSxsZhMRDIAFkRb9U-mgsOT5LLcq4j2Yh-3w130_provenance.
- NP441282.RAQLdf-WPWSxsZhMRDIAFkRb9U-mgsOT5LLcq4j2Yh-3w130_assertion description "[We report here the first identification of a homozygous mutation in MSH6 in a family with childhood-onset brain tumor, lymphoma, colorectal cancer, and neurofibromatosis type 1 phenotype.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP441282.RAQLdf-WPWSxsZhMRDIAFkRb9U-mgsOT5LLcq4j2Yh-3w130_provenance.