Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP954187.RAXoQTqBBvgZdPbhlaNgN1CTrj9drnRdR4Fa69CLmWNbM130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP954187.RAXoQTqBBvgZdPbhlaNgN1CTrj9drnRdR4Fa69CLmWNbM130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP954187.RAXoQTqBBvgZdPbhlaNgN1CTrj9drnRdR4Fa69CLmWNbM130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP954187.RAXoQTqBBvgZdPbhlaNgN1CTrj9drnRdR4Fa69CLmWNbM130_provenance.
- NP954187.RAXoQTqBBvgZdPbhlaNgN1CTrj9drnRdR4Fa69CLmWNbM130_assertion description "[The novel alteration Q944E identified in our study possibly represents a rare disease-related allele, nevertheless functional analysis is still warranted to resolve the ability of this altered BACH1 protein to bind BRCA1.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP954187.RAXoQTqBBvgZdPbhlaNgN1CTrj9drnRdR4Fa69CLmWNbM130_provenance.
- NP954187.RAXoQTqBBvgZdPbhlaNgN1CTrj9drnRdR4Fa69CLmWNbM130_assertion evidence source_evidence_literature NP954187.RAXoQTqBBvgZdPbhlaNgN1CTrj9drnRdR4Fa69CLmWNbM130_provenance.
- NP954187.RAXoQTqBBvgZdPbhlaNgN1CTrj9drnRdR4Fa69CLmWNbM130_assertion SIO_000772 18483852 NP954187.RAXoQTqBBvgZdPbhlaNgN1CTrj9drnRdR4Fa69CLmWNbM130_provenance.
- NP954187.RAXoQTqBBvgZdPbhlaNgN1CTrj9drnRdR4Fa69CLmWNbM130_assertion wasDerivedFrom befree-20150227 NP954187.RAXoQTqBBvgZdPbhlaNgN1CTrj9drnRdR4Fa69CLmWNbM130_provenance.
- NP954187.RAXoQTqBBvgZdPbhlaNgN1CTrj9drnRdR4Fa69CLmWNbM130_assertion wasGeneratedBy ECO_0000203 NP954187.RAXoQTqBBvgZdPbhlaNgN1CTrj9drnRdR4Fa69CLmWNbM130_provenance.
- befree-20150227 importedOn "2015-02-27" NP954187.RAXoQTqBBvgZdPbhlaNgN1CTrj9drnRdR4Fa69CLmWNbM130_provenance.