Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP715605.RAMVHryrQPtuxZq5m5LQviLIAv7_D9gX1cExOYKq8R_P4130_provenance>. }
Showing items 1 to 9 of
9
with 100 items per page.
- source_evidence_literature type ECO_0000212 NP715605.RAMVHryrQPtuxZq5m5LQviLIAv7_D9gX1cExOYKq8R_P4130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP715605.RAMVHryrQPtuxZq5m5LQviLIAv7_D9gX1cExOYKq8R_P4130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP715605.RAMVHryrQPtuxZq5m5LQviLIAv7_D9gX1cExOYKq8R_P4130_provenance.
- NP715605.RAMVHryrQPtuxZq5m5LQviLIAv7_D9gX1cExOYKq8R_P4130_assertion description "[Clinical review of known individuals with MEK1/MEK2 mutations suggests that these patients show dysmorphic features, ectodermal abnormalities and cognitive deficit similar to what was observed in BRAF-mutated patients and in the general CFCS population.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP715605.RAMVHryrQPtuxZq5m5LQviLIAv7_D9gX1cExOYKq8R_P4130_provenance.
- NP715605.RAMVHryrQPtuxZq5m5LQviLIAv7_D9gX1cExOYKq8R_P4130_assertion evidence source_evidence_literature NP715605.RAMVHryrQPtuxZq5m5LQviLIAv7_D9gX1cExOYKq8R_P4130_provenance.
- NP715605.RAMVHryrQPtuxZq5m5LQviLIAv7_D9gX1cExOYKq8R_P4130_assertion SIO_000772 19156172 NP715605.RAMVHryrQPtuxZq5m5LQviLIAv7_D9gX1cExOYKq8R_P4130_provenance.
- NP715605.RAMVHryrQPtuxZq5m5LQviLIAv7_D9gX1cExOYKq8R_P4130_assertion wasDerivedFrom befree-2016 NP715605.RAMVHryrQPtuxZq5m5LQviLIAv7_D9gX1cExOYKq8R_P4130_provenance.
- NP715605.RAMVHryrQPtuxZq5m5LQviLIAv7_D9gX1cExOYKq8R_P4130_assertion wasGeneratedBy ECO_0000203 NP715605.RAMVHryrQPtuxZq5m5LQviLIAv7_D9gX1cExOYKq8R_P4130_provenance.
- befree-2016 importedOn "2016-02-19" NP715605.RAMVHryrQPtuxZq5m5LQviLIAv7_D9gX1cExOYKq8R_P4130_provenance.