Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP412204.RAFljKY9q7MOzc87YAp9BpEI9VsffuXNcycnlw3u3KmgM130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP412204.RAFljKY9q7MOzc87YAp9BpEI9VsffuXNcycnlw3u3KmgM130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP412204.RAFljKY9q7MOzc87YAp9BpEI9VsffuXNcycnlw3u3KmgM130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP412204.RAFljKY9q7MOzc87YAp9BpEI9VsffuXNcycnlw3u3KmgM130_provenance.
- NP412204.RAFljKY9q7MOzc87YAp9BpEI9VsffuXNcycnlw3u3KmgM130_assertion description "[It is suggested that the t(12;22)(q13;q13) is a primary cytogenetic abnormality in clear-cell sarcoma and distinguishes this tumor type from malignant melanoma.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP412204.RAFljKY9q7MOzc87YAp9BpEI9VsffuXNcycnlw3u3KmgM130_provenance.
- NP412204.RAFljKY9q7MOzc87YAp9BpEI9VsffuXNcycnlw3u3KmgM130_assertion evidence source_evidence_literature NP412204.RAFljKY9q7MOzc87YAp9BpEI9VsffuXNcycnlw3u3KmgM130_provenance.
- NP412204.RAFljKY9q7MOzc87YAp9BpEI9VsffuXNcycnlw3u3KmgM130_assertion SIO_000772 1373311 NP412204.RAFljKY9q7MOzc87YAp9BpEI9VsffuXNcycnlw3u3KmgM130_provenance.
- NP412204.RAFljKY9q7MOzc87YAp9BpEI9VsffuXNcycnlw3u3KmgM130_assertion wasDerivedFrom befree-2016 NP412204.RAFljKY9q7MOzc87YAp9BpEI9VsffuXNcycnlw3u3KmgM130_provenance.
- NP412204.RAFljKY9q7MOzc87YAp9BpEI9VsffuXNcycnlw3u3KmgM130_assertion wasGeneratedBy ECO_0000203 NP412204.RAFljKY9q7MOzc87YAp9BpEI9VsffuXNcycnlw3u3KmgM130_provenance.
- befree-2016 importedOn "2016-02-19" NP412204.RAFljKY9q7MOzc87YAp9BpEI9VsffuXNcycnlw3u3KmgM130_provenance.