Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP320165.RADOzftVZqeoTqFMlsvTgB8xKoT_eKFh6eXs8mOtibSVg130_provenance>. }
Showing items 1 to 9 of
9
with 100 items per page.
- source_evidence_literature type ECO_0000212 NP320165.RADOzftVZqeoTqFMlsvTgB8xKoT_eKFh6eXs8mOtibSVg130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP320165.RADOzftVZqeoTqFMlsvTgB8xKoT_eKFh6eXs8mOtibSVg130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP320165.RADOzftVZqeoTqFMlsvTgB8xKoT_eKFh6eXs8mOtibSVg130_provenance.
- befree-20150227 importedOn "2015-02-27" NP320165.RADOzftVZqeoTqFMlsvTgB8xKoT_eKFh6eXs8mOtibSVg130_provenance.
- NP320165.RADOzftVZqeoTqFMlsvTgB8xKoT_eKFh6eXs8mOtibSVg130_assertion wasGeneratedBy ECO_0000203 NP320165.RADOzftVZqeoTqFMlsvTgB8xKoT_eKFh6eXs8mOtibSVg130_provenance.
- NP320165.RADOzftVZqeoTqFMlsvTgB8xKoT_eKFh6eXs8mOtibSVg130_assertion wasDerivedFrom befree-20150227 NP320165.RADOzftVZqeoTqFMlsvTgB8xKoT_eKFh6eXs8mOtibSVg130_provenance.
- NP320165.RADOzftVZqeoTqFMlsvTgB8xKoT_eKFh6eXs8mOtibSVg130_assertion SIO_000772 23720012 NP320165.RADOzftVZqeoTqFMlsvTgB8xKoT_eKFh6eXs8mOtibSVg130_provenance.
- NP320165.RADOzftVZqeoTqFMlsvTgB8xKoT_eKFh6eXs8mOtibSVg130_assertion evidence source_evidence_literature NP320165.RADOzftVZqeoTqFMlsvTgB8xKoT_eKFh6eXs8mOtibSVg130_provenance.
- NP320165.RADOzftVZqeoTqFMlsvTgB8xKoT_eKFh6eXs8mOtibSVg130_assertion description "[The major genetic testing laboratories for X-linked Alport syndrome worldwide have established a Web-based database for published and unpublished COL4A5 variants ( https://grenada.lumc.nl/LOVD2/COL4A/home.php?select_db=COL4A5 ).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP320165.RADOzftVZqeoTqFMlsvTgB8xKoT_eKFh6eXs8mOtibSVg130_provenance.