Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP722767.RAPc3UhMo7hOHBbj1nKr-tIYAp05xnbiQW0QstY3ptYWw130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP722767.RAPc3UhMo7hOHBbj1nKr-tIYAp05xnbiQW0QstY3ptYWw130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP722767.RAPc3UhMo7hOHBbj1nKr-tIYAp05xnbiQW0QstY3ptYWw130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP722767.RAPc3UhMo7hOHBbj1nKr-tIYAp05xnbiQW0QstY3ptYWw130_provenance.
- NP722767.RAPc3UhMo7hOHBbj1nKr-tIYAp05xnbiQW0QstY3ptYWw130_assertion description "[In summary, immunohistochemistry with ALK1 antibody allows the identification of a distinct subgroup within the ALCL of T or null phenotype that is associated with 2p23 abnormalities and lacks the marked histological pleomorphism described in ALCL in general.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP722767.RAPc3UhMo7hOHBbj1nKr-tIYAp05xnbiQW0QstY3ptYWw130_provenance.
- NP722767.RAPc3UhMo7hOHBbj1nKr-tIYAp05xnbiQW0QstY3ptYWw130_assertion evidence source_evidence_literature NP722767.RAPc3UhMo7hOHBbj1nKr-tIYAp05xnbiQW0QstY3ptYWw130_provenance.
- NP722767.RAPc3UhMo7hOHBbj1nKr-tIYAp05xnbiQW0QstY3ptYWw130_assertion SIO_000772 9250148 NP722767.RAPc3UhMo7hOHBbj1nKr-tIYAp05xnbiQW0QstY3ptYWw130_provenance.
- NP722767.RAPc3UhMo7hOHBbj1nKr-tIYAp05xnbiQW0QstY3ptYWw130_assertion wasDerivedFrom befree-20140225 NP722767.RAPc3UhMo7hOHBbj1nKr-tIYAp05xnbiQW0QstY3ptYWw130_provenance.
- NP722767.RAPc3UhMo7hOHBbj1nKr-tIYAp05xnbiQW0QstY3ptYWw130_assertion wasGeneratedBy ECO_0000203 NP722767.RAPc3UhMo7hOHBbj1nKr-tIYAp05xnbiQW0QstY3ptYWw130_provenance.
- befree-20140225 importedOn "2014-02-25" NP722767.RAPc3UhMo7hOHBbj1nKr-tIYAp05xnbiQW0QstY3ptYWw130_provenance.