Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP1246468.RAjSwfJXjgH_s6o0PcYZde67blZnVotFhR-KXx0ndbXLo130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP1246468.RAjSwfJXjgH_s6o0PcYZde67blZnVotFhR-KXx0ndbXLo130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP1246468.RAjSwfJXjgH_s6o0PcYZde67blZnVotFhR-KXx0ndbXLo130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP1246468.RAjSwfJXjgH_s6o0PcYZde67blZnVotFhR-KXx0ndbXLo130_provenance.
- NP1246468.RAjSwfJXjgH_s6o0PcYZde67blZnVotFhR-KXx0ndbXLo130_assertion description "[Using a TruSeq amplicon cancer panel, this study evaluated 48 familial MBCs (3 BRCA1 germline mutant, 17 BRCA2 germline mutant and 28 BRCAX) for hotspot somatic mutations and copy number changes in 48 common cancer genes.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1246468.RAjSwfJXjgH_s6o0PcYZde67blZnVotFhR-KXx0ndbXLo130_provenance.
- NP1246468.RAjSwfJXjgH_s6o0PcYZde67blZnVotFhR-KXx0ndbXLo130_assertion evidence source_evidence_literature NP1246468.RAjSwfJXjgH_s6o0PcYZde67blZnVotFhR-KXx0ndbXLo130_provenance.
- NP1246468.RAjSwfJXjgH_s6o0PcYZde67blZnVotFhR-KXx0ndbXLo130_assertion SIO_000772 25490678 NP1246468.RAjSwfJXjgH_s6o0PcYZde67blZnVotFhR-KXx0ndbXLo130_provenance.
- NP1246468.RAjSwfJXjgH_s6o0PcYZde67blZnVotFhR-KXx0ndbXLo130_assertion wasDerivedFrom befree-2016 NP1246468.RAjSwfJXjgH_s6o0PcYZde67blZnVotFhR-KXx0ndbXLo130_provenance.
- NP1246468.RAjSwfJXjgH_s6o0PcYZde67blZnVotFhR-KXx0ndbXLo130_assertion wasGeneratedBy ECO_0000203 NP1246468.RAjSwfJXjgH_s6o0PcYZde67blZnVotFhR-KXx0ndbXLo130_provenance.
- befree-2016 importedOn "2016-02-19" NP1246468.RAjSwfJXjgH_s6o0PcYZde67blZnVotFhR-KXx0ndbXLo130_provenance.