Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP845759.RAJETDrl0fzQO9Mb_MFN5xrqunDQaX4ZXe7rD5lyhKPkk130_provenance>. }
Showing items 1 to 9 of
9
with 100 items per page.
- source_evidence_literature type ECO_0000212 NP845759.RAJETDrl0fzQO9Mb_MFN5xrqunDQaX4ZXe7rD5lyhKPkk130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP845759.RAJETDrl0fzQO9Mb_MFN5xrqunDQaX4ZXe7rD5lyhKPkk130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP845759.RAJETDrl0fzQO9Mb_MFN5xrqunDQaX4ZXe7rD5lyhKPkk130_provenance.
- befree-20150227 importedOn "2015-02-27" NP845759.RAJETDrl0fzQO9Mb_MFN5xrqunDQaX4ZXe7rD5lyhKPkk130_provenance.
- NP845759.RAJETDrl0fzQO9Mb_MFN5xrqunDQaX4ZXe7rD5lyhKPkk130_assertion wasGeneratedBy ECO_0000203 NP845759.RAJETDrl0fzQO9Mb_MFN5xrqunDQaX4ZXe7rD5lyhKPkk130_provenance.
- NP845759.RAJETDrl0fzQO9Mb_MFN5xrqunDQaX4ZXe7rD5lyhKPkk130_assertion wasDerivedFrom befree-20150227 NP845759.RAJETDrl0fzQO9Mb_MFN5xrqunDQaX4ZXe7rD5lyhKPkk130_provenance.
- NP845759.RAJETDrl0fzQO9Mb_MFN5xrqunDQaX4ZXe7rD5lyhKPkk130_assertion SIO_000772 11705868 NP845759.RAJETDrl0fzQO9Mb_MFN5xrqunDQaX4ZXe7rD5lyhKPkk130_provenance.
- NP845759.RAJETDrl0fzQO9Mb_MFN5xrqunDQaX4ZXe7rD5lyhKPkk130_assertion evidence source_evidence_literature NP845759.RAJETDrl0fzQO9Mb_MFN5xrqunDQaX4ZXe7rD5lyhKPkk130_provenance.
- NP845759.RAJETDrl0fzQO9Mb_MFN5xrqunDQaX4ZXe7rD5lyhKPkk130_assertion description "[This is the first report of genetic alterations in the spn gene in a human malignancy and suggests that genetic alterations in spn and the resulting immunohistochemical phenotypes based on SPN subcellular localization in CRCs may be useful in determining prognosis of patients with subtypes of CRC.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP845759.RAJETDrl0fzQO9Mb_MFN5xrqunDQaX4ZXe7rD5lyhKPkk130_provenance.