Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP419011.RAeQ3VVe_E-Dgr0y2Vyw7N9QSEtaD3-2roM8AX_D_sSPw130_provenance>. }
Showing items 1 to 9 of
9
with 100 items per page.
- source_evidence_literature type ECO_0000212 NP419011.RAeQ3VVe_E-Dgr0y2Vyw7N9QSEtaD3-2roM8AX_D_sSPw130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP419011.RAeQ3VVe_E-Dgr0y2Vyw7N9QSEtaD3-2roM8AX_D_sSPw130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP419011.RAeQ3VVe_E-Dgr0y2Vyw7N9QSEtaD3-2roM8AX_D_sSPw130_provenance.
- NP419011.RAeQ3VVe_E-Dgr0y2Vyw7N9QSEtaD3-2roM8AX_D_sSPw130_assertion description "[The purpose of this study was to investigate the cytogenetic abnormalities present in a series of 13 CD30+ CTCL samples obtained from nine patients fulfilling both EORTC and WHO diagnostic criteria, by the use of comparative genomic hybridization (CGH).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP419011.RAeQ3VVe_E-Dgr0y2Vyw7N9QSEtaD3-2roM8AX_D_sSPw130_provenance.
- NP419011.RAeQ3VVe_E-Dgr0y2Vyw7N9QSEtaD3-2roM8AX_D_sSPw130_assertion evidence source_evidence_literature NP419011.RAeQ3VVe_E-Dgr0y2Vyw7N9QSEtaD3-2roM8AX_D_sSPw130_provenance.
- NP419011.RAeQ3VVe_E-Dgr0y2Vyw7N9QSEtaD3-2roM8AX_D_sSPw130_assertion SIO_000772 14595754 NP419011.RAeQ3VVe_E-Dgr0y2Vyw7N9QSEtaD3-2roM8AX_D_sSPw130_provenance.
- NP419011.RAeQ3VVe_E-Dgr0y2Vyw7N9QSEtaD3-2roM8AX_D_sSPw130_assertion wasDerivedFrom befree-2016 NP419011.RAeQ3VVe_E-Dgr0y2Vyw7N9QSEtaD3-2roM8AX_D_sSPw130_provenance.
- NP419011.RAeQ3VVe_E-Dgr0y2Vyw7N9QSEtaD3-2roM8AX_D_sSPw130_assertion wasGeneratedBy ECO_0000203 NP419011.RAeQ3VVe_E-Dgr0y2Vyw7N9QSEtaD3-2roM8AX_D_sSPw130_provenance.
- befree-2016 importedOn "2016-02-19" NP419011.RAeQ3VVe_E-Dgr0y2Vyw7N9QSEtaD3-2roM8AX_D_sSPw130_provenance.