Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP820395.RA6TMCxJn4ZBHoX4O6ivCdiJjIauWnXZohl8t8_pdUy4k130_provenance>. }
Showing items 1 to 9 of
9
with 100 items per page.
- source_evidence_literature type ECO_0000212 NP820395.RA6TMCxJn4ZBHoX4O6ivCdiJjIauWnXZohl8t8_pdUy4k130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP820395.RA6TMCxJn4ZBHoX4O6ivCdiJjIauWnXZohl8t8_pdUy4k130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP820395.RA6TMCxJn4ZBHoX4O6ivCdiJjIauWnXZohl8t8_pdUy4k130_provenance.
- NP820395.RA6TMCxJn4ZBHoX4O6ivCdiJjIauWnXZohl8t8_pdUy4k130_assertion description "[CEDNIK (cerebral dysgenesis, neuropathy, ichthyosis and keratoderma) syndrome is a rare genodermatosis which was shown 5 years ago in one family to be associated with a loss-of-function mutation in SNAP29, encoding a member of the SNARE family of proteins.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP820395.RA6TMCxJn4ZBHoX4O6ivCdiJjIauWnXZohl8t8_pdUy4k130_provenance.
- NP820395.RA6TMCxJn4ZBHoX4O6ivCdiJjIauWnXZohl8t8_pdUy4k130_assertion evidence source_evidence_literature NP820395.RA6TMCxJn4ZBHoX4O6ivCdiJjIauWnXZohl8t8_pdUy4k130_provenance.
- NP820395.RA6TMCxJn4ZBHoX4O6ivCdiJjIauWnXZohl8t8_pdUy4k130_assertion SIO_000772 21073448 NP820395.RA6TMCxJn4ZBHoX4O6ivCdiJjIauWnXZohl8t8_pdUy4k130_provenance.
- NP820395.RA6TMCxJn4ZBHoX4O6ivCdiJjIauWnXZohl8t8_pdUy4k130_assertion wasDerivedFrom befree-20150227 NP820395.RA6TMCxJn4ZBHoX4O6ivCdiJjIauWnXZohl8t8_pdUy4k130_provenance.
- NP820395.RA6TMCxJn4ZBHoX4O6ivCdiJjIauWnXZohl8t8_pdUy4k130_assertion wasGeneratedBy ECO_0000203 NP820395.RA6TMCxJn4ZBHoX4O6ivCdiJjIauWnXZohl8t8_pdUy4k130_provenance.
- befree-20150227 importedOn "2015-02-27" NP820395.RA6TMCxJn4ZBHoX4O6ivCdiJjIauWnXZohl8t8_pdUy4k130_provenance.