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- source_evidence_literature type ECO_0000212 NP934814.RAxqripFcmr6Fm7Zs7G7-_B1D-NE1SZGgLbqe0bYVkdwg130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP934814.RAxqripFcmr6Fm7Zs7G7-_B1D-NE1SZGgLbqe0bYVkdwg130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP934814.RAxqripFcmr6Fm7Zs7G7-_B1D-NE1SZGgLbqe0bYVkdwg130_provenance.
- NP934814.RAxqripFcmr6Fm7Zs7G7-_B1D-NE1SZGgLbqe0bYVkdwg130_assertion description "[Recent advances in genetics have resulted in the identification of missense mutations in TRPV4 in patients with these hereditary neuropathies.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP934814.RAxqripFcmr6Fm7Zs7G7-_B1D-NE1SZGgLbqe0bYVkdwg130_provenance.
- NP934814.RAxqripFcmr6Fm7Zs7G7-_B1D-NE1SZGgLbqe0bYVkdwg130_assertion evidence source_evidence_literature NP934814.RAxqripFcmr6Fm7Zs7G7-_B1D-NE1SZGgLbqe0bYVkdwg130_provenance.
- NP934814.RAxqripFcmr6Fm7Zs7G7-_B1D-NE1SZGgLbqe0bYVkdwg130_assertion SIO_000772 22187434 NP934814.RAxqripFcmr6Fm7Zs7G7-_B1D-NE1SZGgLbqe0bYVkdwg130_provenance.
- NP934814.RAxqripFcmr6Fm7Zs7G7-_B1D-NE1SZGgLbqe0bYVkdwg130_assertion wasDerivedFrom befree-20140225 NP934814.RAxqripFcmr6Fm7Zs7G7-_B1D-NE1SZGgLbqe0bYVkdwg130_provenance.
- NP934814.RAxqripFcmr6Fm7Zs7G7-_B1D-NE1SZGgLbqe0bYVkdwg130_assertion wasGeneratedBy ECO_0000203 NP934814.RAxqripFcmr6Fm7Zs7G7-_B1D-NE1SZGgLbqe0bYVkdwg130_provenance.
- befree-20140225 importedOn "2014-02-25" NP934814.RAxqripFcmr6Fm7Zs7G7-_B1D-NE1SZGgLbqe0bYVkdwg130_provenance.