Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP829275.RAVGC-zOKe5csX9Kny3fZSdggCILtuzDw47WUmU3cKW-I130_provenance>. }
Showing items 1 to 9 of
9
with 100 items per page.
- source_evidence_literature type ECO_0000212 NP829275.RAVGC-zOKe5csX9Kny3fZSdggCILtuzDw47WUmU3cKW-I130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP829275.RAVGC-zOKe5csX9Kny3fZSdggCILtuzDw47WUmU3cKW-I130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP829275.RAVGC-zOKe5csX9Kny3fZSdggCILtuzDw47WUmU3cKW-I130_provenance.
- NP829275.RAVGC-zOKe5csX9Kny3fZSdggCILtuzDw47WUmU3cKW-I130_assertion description "[Mutations in FBN1, ADAMTS10, or ADAMTS17 cause Weill-Marchesani syndrome by disrupting the microfibrillar environment, while geleophysic dysplasia is associated with enhanced TGF-? signaling mediated through mutations in FBN1 or ADAMTSL2.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP829275.RAVGC-zOKe5csX9Kny3fZSdggCILtuzDw47WUmU3cKW-I130_provenance.
- NP829275.RAVGC-zOKe5csX9Kny3fZSdggCILtuzDw47WUmU3cKW-I130_assertion evidence source_evidence_literature NP829275.RAVGC-zOKe5csX9Kny3fZSdggCILtuzDw47WUmU3cKW-I130_provenance.
- NP829275.RAVGC-zOKe5csX9Kny3fZSdggCILtuzDw47WUmU3cKW-I130_assertion SIO_000772 24214363 NP829275.RAVGC-zOKe5csX9Kny3fZSdggCILtuzDw47WUmU3cKW-I130_provenance.
- NP829275.RAVGC-zOKe5csX9Kny3fZSdggCILtuzDw47WUmU3cKW-I130_assertion wasDerivedFrom befree-20150227 NP829275.RAVGC-zOKe5csX9Kny3fZSdggCILtuzDw47WUmU3cKW-I130_provenance.
- NP829275.RAVGC-zOKe5csX9Kny3fZSdggCILtuzDw47WUmU3cKW-I130_assertion wasGeneratedBy ECO_0000203 NP829275.RAVGC-zOKe5csX9Kny3fZSdggCILtuzDw47WUmU3cKW-I130_provenance.
- befree-20150227 importedOn "2015-02-27" NP829275.RAVGC-zOKe5csX9Kny3fZSdggCILtuzDw47WUmU3cKW-I130_provenance.