Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP1296072.RAspLoPS2FLa66GQWDe9a8CqiLE9LqElpTxRoCj9eqVd0130_provenance>. }
Showing items 1 to 9 of
9
with 100 items per page.
- source_evidence_literature type ECO_0000212 NP1296072.RAspLoPS2FLa66GQWDe9a8CqiLE9LqElpTxRoCj9eqVd0130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP1296072.RAspLoPS2FLa66GQWDe9a8CqiLE9LqElpTxRoCj9eqVd0130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP1296072.RAspLoPS2FLa66GQWDe9a8CqiLE9LqElpTxRoCj9eqVd0130_provenance.
- NP1296072.RAspLoPS2FLa66GQWDe9a8CqiLE9LqElpTxRoCj9eqVd0130_assertion description "[The conclusion that most variants of OI are caused by mutations in the structural genes for type I procollagen has broad implications for other diseases that affect connective tissue, diseases such as chondrodystrophies, osteoarthritis, and osteoporosis.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1296072.RAspLoPS2FLa66GQWDe9a8CqiLE9LqElpTxRoCj9eqVd0130_provenance.
- NP1296072.RAspLoPS2FLa66GQWDe9a8CqiLE9LqElpTxRoCj9eqVd0130_assertion evidence source_evidence_literature NP1296072.RAspLoPS2FLa66GQWDe9a8CqiLE9LqElpTxRoCj9eqVd0130_provenance.
- NP1296072.RAspLoPS2FLa66GQWDe9a8CqiLE9LqElpTxRoCj9eqVd0130_assertion SIO_000772 2683782 NP1296072.RAspLoPS2FLa66GQWDe9a8CqiLE9LqElpTxRoCj9eqVd0130_provenance.
- NP1296072.RAspLoPS2FLa66GQWDe9a8CqiLE9LqElpTxRoCj9eqVd0130_assertion wasDerivedFrom befree-2016 NP1296072.RAspLoPS2FLa66GQWDe9a8CqiLE9LqElpTxRoCj9eqVd0130_provenance.
- NP1296072.RAspLoPS2FLa66GQWDe9a8CqiLE9LqElpTxRoCj9eqVd0130_assertion wasGeneratedBy ECO_0000203 NP1296072.RAspLoPS2FLa66GQWDe9a8CqiLE9LqElpTxRoCj9eqVd0130_provenance.
- befree-2016 importedOn "2016-02-19" NP1296072.RAspLoPS2FLa66GQWDe9a8CqiLE9LqElpTxRoCj9eqVd0130_provenance.