Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP958151.RAzQ4qXe403xvX-WeC9_1HHtlrrO22N9hz0c-PeC2kj8E130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP958151.RAzQ4qXe403xvX-WeC9_1HHtlrrO22N9hz0c-PeC2kj8E130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP958151.RAzQ4qXe403xvX-WeC9_1HHtlrrO22N9hz0c-PeC2kj8E130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP958151.RAzQ4qXe403xvX-WeC9_1HHtlrrO22N9hz0c-PeC2kj8E130_provenance.
- NP958151.RAzQ4qXe403xvX-WeC9_1HHtlrrO22N9hz0c-PeC2kj8E130_assertion description "[Taken together, our results demonstrate the robust performance of VarScan 2 for somatic mutation and CNA detection and shed new light on the landscape of genetic alterations in ovarian cancer.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP958151.RAzQ4qXe403xvX-WeC9_1HHtlrrO22N9hz0c-PeC2kj8E130_provenance.
- NP958151.RAzQ4qXe403xvX-WeC9_1HHtlrrO22N9hz0c-PeC2kj8E130_assertion evidence source_evidence_literature NP958151.RAzQ4qXe403xvX-WeC9_1HHtlrrO22N9hz0c-PeC2kj8E130_provenance.
- NP958151.RAzQ4qXe403xvX-WeC9_1HHtlrrO22N9hz0c-PeC2kj8E130_assertion SIO_000772 22300766 NP958151.RAzQ4qXe403xvX-WeC9_1HHtlrrO22N9hz0c-PeC2kj8E130_provenance.
- NP958151.RAzQ4qXe403xvX-WeC9_1HHtlrrO22N9hz0c-PeC2kj8E130_assertion wasDerivedFrom befree-2016 NP958151.RAzQ4qXe403xvX-WeC9_1HHtlrrO22N9hz0c-PeC2kj8E130_provenance.
- NP958151.RAzQ4qXe403xvX-WeC9_1HHtlrrO22N9hz0c-PeC2kj8E130_assertion wasGeneratedBy ECO_0000203 NP958151.RAzQ4qXe403xvX-WeC9_1HHtlrrO22N9hz0c-PeC2kj8E130_provenance.
- befree-2016 importedOn "2016-02-19" NP958151.RAzQ4qXe403xvX-WeC9_1HHtlrrO22N9hz0c-PeC2kj8E130_provenance.