Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP56785.RAQSuXcWRnFLtQwgnCg2VwP4F9aj1nxikVbZa5HElpICA130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP56785.RAQSuXcWRnFLtQwgnCg2VwP4F9aj1nxikVbZa5HElpICA130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP56785.RAQSuXcWRnFLtQwgnCg2VwP4F9aj1nxikVbZa5HElpICA130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP56785.RAQSuXcWRnFLtQwgnCg2VwP4F9aj1nxikVbZa5HElpICA130_provenance.
- NP56785.RAQSuXcWRnFLtQwgnCg2VwP4F9aj1nxikVbZa5HElpICA130_assertion description "[Homozygous deletions were more frequent in melanoma cell lines than in melanoma tumors in p21, p16 and p15 (22.2%, 44.4%, and 44.4% versus 7.7%, 2.5%, and 5.1% respectively).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP56785.RAQSuXcWRnFLtQwgnCg2VwP4F9aj1nxikVbZa5HElpICA130_provenance.
- NP56785.RAQSuXcWRnFLtQwgnCg2VwP4F9aj1nxikVbZa5HElpICA130_assertion evidence source_evidence_literature NP56785.RAQSuXcWRnFLtQwgnCg2VwP4F9aj1nxikVbZa5HElpICA130_provenance.
- NP56785.RAQSuXcWRnFLtQwgnCg2VwP4F9aj1nxikVbZa5HElpICA130_assertion SIO_000772 15960923 NP56785.RAQSuXcWRnFLtQwgnCg2VwP4F9aj1nxikVbZa5HElpICA130_provenance.
- NP56785.RAQSuXcWRnFLtQwgnCg2VwP4F9aj1nxikVbZa5HElpICA130_assertion wasDerivedFrom gad-20150221 NP56785.RAQSuXcWRnFLtQwgnCg2VwP4F9aj1nxikVbZa5HElpICA130_provenance.
- NP56785.RAQSuXcWRnFLtQwgnCg2VwP4F9aj1nxikVbZa5HElpICA130_assertion wasGeneratedBy ECO_0000203 NP56785.RAQSuXcWRnFLtQwgnCg2VwP4F9aj1nxikVbZa5HElpICA130_provenance.
- gad-20150221 importedOn "2015-02-21" NP56785.RAQSuXcWRnFLtQwgnCg2VwP4F9aj1nxikVbZa5HElpICA130_provenance.