Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP108007.RAw2ew00_MkcnPg5G7FGZ3_gWgoEg13C6LJb2i9wkoCjs130_provenance>. }
Showing items 1 to 9 of
9
with 100 items per page.
- source_evidence_literature type ECO_0000212 NP108007.RAw2ew00_MkcnPg5G7FGZ3_gWgoEg13C6LJb2i9wkoCjs130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP108007.RAw2ew00_MkcnPg5G7FGZ3_gWgoEg13C6LJb2i9wkoCjs130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP108007.RAw2ew00_MkcnPg5G7FGZ3_gWgoEg13C6LJb2i9wkoCjs130_provenance.
- NP108007.RAw2ew00_MkcnPg5G7FGZ3_gWgoEg13C6LJb2i9wkoCjs130_assertion description "[PC deficiency was frequent in pediatric PVT patients and does not seem to be an inherited condition.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP108007.RAw2ew00_MkcnPg5G7FGZ3_gWgoEg13C6LJb2i9wkoCjs130_provenance.
- NP108007.RAw2ew00_MkcnPg5G7FGZ3_gWgoEg13C6LJb2i9wkoCjs130_assertion evidence source_evidence_literature NP108007.RAw2ew00_MkcnPg5G7FGZ3_gWgoEg13C6LJb2i9wkoCjs130_provenance.
- NP108007.RAw2ew00_MkcnPg5G7FGZ3_gWgoEg13C6LJb2i9wkoCjs130_assertion SIO_000772 15359390 NP108007.RAw2ew00_MkcnPg5G7FGZ3_gWgoEg13C6LJb2i9wkoCjs130_provenance.
- NP108007.RAw2ew00_MkcnPg5G7FGZ3_gWgoEg13C6LJb2i9wkoCjs130_assertion wasDerivedFrom gad-20150221 NP108007.RAw2ew00_MkcnPg5G7FGZ3_gWgoEg13C6LJb2i9wkoCjs130_provenance.
- NP108007.RAw2ew00_MkcnPg5G7FGZ3_gWgoEg13C6LJb2i9wkoCjs130_assertion wasGeneratedBy ECO_0000203 NP108007.RAw2ew00_MkcnPg5G7FGZ3_gWgoEg13C6LJb2i9wkoCjs130_provenance.
- gad-20150221 importedOn "2015-02-21" NP108007.RAw2ew00_MkcnPg5G7FGZ3_gWgoEg13C6LJb2i9wkoCjs130_provenance.