Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP1126826.RAG0G1H70oYfGDa2ONMRf7gv4XK0dT4inISRrqZefHozU130_provenance>. }
Showing items 1 to 9 of
9
with 100 items per page.
- source_evidence_literature type ECO_0000212 NP1126826.RAG0G1H70oYfGDa2ONMRf7gv4XK0dT4inISRrqZefHozU130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP1126826.RAG0G1H70oYfGDa2ONMRf7gv4XK0dT4inISRrqZefHozU130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP1126826.RAG0G1H70oYfGDa2ONMRf7gv4XK0dT4inISRrqZefHozU130_provenance.
- NP1126826.RAG0G1H70oYfGDa2ONMRf7gv4XK0dT4inISRrqZefHozU130_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." NP1126826.RAG0G1H70oYfGDa2ONMRf7gv4XK0dT4inISRrqZefHozU130_provenance.
- NP1126826.RAG0G1H70oYfGDa2ONMRf7gv4XK0dT4inISRrqZefHozU130_assertion evidence source_evidence_literature NP1126826.RAG0G1H70oYfGDa2ONMRf7gv4XK0dT4inISRrqZefHozU130_provenance.
- NP1126826.RAG0G1H70oYfGDa2ONMRf7gv4XK0dT4inISRrqZefHozU130_assertion SIO_000772 24214363 NP1126826.RAG0G1H70oYfGDa2ONMRf7gv4XK0dT4inISRrqZefHozU130_provenance.
- NP1126826.RAG0G1H70oYfGDa2ONMRf7gv4XK0dT4inISRrqZefHozU130_assertion wasDerivedFrom befree-2016 NP1126826.RAG0G1H70oYfGDa2ONMRf7gv4XK0dT4inISRrqZefHozU130_provenance.
- NP1126826.RAG0G1H70oYfGDa2ONMRf7gv4XK0dT4inISRrqZefHozU130_assertion wasGeneratedBy ECO_0000203 NP1126826.RAG0G1H70oYfGDa2ONMRf7gv4XK0dT4inISRrqZefHozU130_provenance.
- befree-2016 importedOn "2016-02-19" NP1126826.RAG0G1H70oYfGDa2ONMRf7gv4XK0dT4inISRrqZefHozU130_provenance.