Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP715606.RAhrm0CK149IEqZNQAcBFGOuRHiW9Lx016RWqpTO7Rp08130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP715606.RAhrm0CK149IEqZNQAcBFGOuRHiW9Lx016RWqpTO7Rp08130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP715606.RAhrm0CK149IEqZNQAcBFGOuRHiW9Lx016RWqpTO7Rp08130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP715606.RAhrm0CK149IEqZNQAcBFGOuRHiW9Lx016RWqpTO7Rp08130_provenance.
- NP715606.RAhrm0CK149IEqZNQAcBFGOuRHiW9Lx016RWqpTO7Rp08130_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." NP715606.RAhrm0CK149IEqZNQAcBFGOuRHiW9Lx016RWqpTO7Rp08130_provenance.
- NP715606.RAhrm0CK149IEqZNQAcBFGOuRHiW9Lx016RWqpTO7Rp08130_assertion evidence source_evidence_literature NP715606.RAhrm0CK149IEqZNQAcBFGOuRHiW9Lx016RWqpTO7Rp08130_provenance.
- NP715606.RAhrm0CK149IEqZNQAcBFGOuRHiW9Lx016RWqpTO7Rp08130_assertion SIO_000772 19156172 NP715606.RAhrm0CK149IEqZNQAcBFGOuRHiW9Lx016RWqpTO7Rp08130_provenance.
- NP715606.RAhrm0CK149IEqZNQAcBFGOuRHiW9Lx016RWqpTO7Rp08130_assertion wasDerivedFrom befree-2016 NP715606.RAhrm0CK149IEqZNQAcBFGOuRHiW9Lx016RWqpTO7Rp08130_provenance.
- NP715606.RAhrm0CK149IEqZNQAcBFGOuRHiW9Lx016RWqpTO7Rp08130_assertion wasGeneratedBy ECO_0000203 NP715606.RAhrm0CK149IEqZNQAcBFGOuRHiW9Lx016RWqpTO7Rp08130_provenance.
- befree-2016 importedOn "2016-02-19" NP715606.RAhrm0CK149IEqZNQAcBFGOuRHiW9Lx016RWqpTO7Rp08130_provenance.