Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP254418.RAbtMUILw09b5sHd8v3hGQZsHHC9_eoy-FEkUMHTWVivs130_provenance>. }
Showing items 1 to 9 of
9
with 100 items per page.
- source_evidence_literature type ECO_0000212 NP254418.RAbtMUILw09b5sHd8v3hGQZsHHC9_eoy-FEkUMHTWVivs130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP254418.RAbtMUILw09b5sHd8v3hGQZsHHC9_eoy-FEkUMHTWVivs130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP254418.RAbtMUILw09b5sHd8v3hGQZsHHC9_eoy-FEkUMHTWVivs130_provenance.
- NP254418.RAbtMUILw09b5sHd8v3hGQZsHHC9_eoy-FEkUMHTWVivs130_assertion description "[This contention is further supported by the discovery that mutations in genes that encode components of the muscle contractile complex (MYH3, TPM2, TNNT3, TNNI2, and MYH8) cause congenital contractures, including clubfoot, in distal arthrogryposis (DA) syndromes.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP254418.RAbtMUILw09b5sHd8v3hGQZsHHC9_eoy-FEkUMHTWVivs130_provenance.
- NP254418.RAbtMUILw09b5sHd8v3hGQZsHHC9_eoy-FEkUMHTWVivs130_assertion evidence source_evidence_literature NP254418.RAbtMUILw09b5sHd8v3hGQZsHHC9_eoy-FEkUMHTWVivs130_provenance.
- NP254418.RAbtMUILw09b5sHd8v3hGQZsHHC9_eoy-FEkUMHTWVivs130_assertion SIO_000772 21834041 NP254418.RAbtMUILw09b5sHd8v3hGQZsHHC9_eoy-FEkUMHTWVivs130_provenance.
- NP254418.RAbtMUILw09b5sHd8v3hGQZsHHC9_eoy-FEkUMHTWVivs130_assertion wasDerivedFrom befree-20140225 NP254418.RAbtMUILw09b5sHd8v3hGQZsHHC9_eoy-FEkUMHTWVivs130_provenance.
- NP254418.RAbtMUILw09b5sHd8v3hGQZsHHC9_eoy-FEkUMHTWVivs130_assertion wasGeneratedBy ECO_0000203 NP254418.RAbtMUILw09b5sHd8v3hGQZsHHC9_eoy-FEkUMHTWVivs130_provenance.
- befree-20140225 importedOn "2014-02-25" NP254418.RAbtMUILw09b5sHd8v3hGQZsHHC9_eoy-FEkUMHTWVivs130_provenance.