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- source_evidence_literature type ECO_0000212 NP795730.RABu66wCoPeauTonMH6r8opyY8pd4fE3Up3VvkN4ZY-tc130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP795730.RABu66wCoPeauTonMH6r8opyY8pd4fE3Up3VvkN4ZY-tc130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP795730.RABu66wCoPeauTonMH6r8opyY8pd4fE3Up3VvkN4ZY-tc130_provenance.
- NP795730.RABu66wCoPeauTonMH6r8opyY8pd4fE3Up3VvkN4ZY-tc130_assertion description "[Their importance is underscored by fibrillin-1 mutations responsible for Marfan syndrome, but their respective roles are still incompletely understood.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP795730.RABu66wCoPeauTonMH6r8opyY8pd4fE3Up3VvkN4ZY-tc130_provenance.
- NP795730.RABu66wCoPeauTonMH6r8opyY8pd4fE3Up3VvkN4ZY-tc130_assertion evidence source_evidence_literature NP795730.RABu66wCoPeauTonMH6r8opyY8pd4fE3Up3VvkN4ZY-tc130_provenance.
- NP795730.RABu66wCoPeauTonMH6r8opyY8pd4fE3Up3VvkN4ZY-tc130_assertion SIO_000772 20179738 NP795730.RABu66wCoPeauTonMH6r8opyY8pd4fE3Up3VvkN4ZY-tc130_provenance.
- NP795730.RABu66wCoPeauTonMH6r8opyY8pd4fE3Up3VvkN4ZY-tc130_assertion wasDerivedFrom befree-2016 NP795730.RABu66wCoPeauTonMH6r8opyY8pd4fE3Up3VvkN4ZY-tc130_provenance.
- NP795730.RABu66wCoPeauTonMH6r8opyY8pd4fE3Up3VvkN4ZY-tc130_assertion wasGeneratedBy ECO_0000203 NP795730.RABu66wCoPeauTonMH6r8opyY8pd4fE3Up3VvkN4ZY-tc130_provenance.
- befree-2016 importedOn "2016-02-19" NP795730.RABu66wCoPeauTonMH6r8opyY8pd4fE3Up3VvkN4ZY-tc130_provenance.