Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP963611.RA9z32HzVIIY0c-Inzf9jpPRipvLcKmB5JIuBQPPM8mZE130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP963611.RA9z32HzVIIY0c-Inzf9jpPRipvLcKmB5JIuBQPPM8mZE130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP963611.RA9z32HzVIIY0c-Inzf9jpPRipvLcKmB5JIuBQPPM8mZE130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP963611.RA9z32HzVIIY0c-Inzf9jpPRipvLcKmB5JIuBQPPM8mZE130_provenance.
- NP963611.RA9z32HzVIIY0c-Inzf9jpPRipvLcKmB5JIuBQPPM8mZE130_assertion description "[We now show that point mutations in the cytoplasmic domain that modify a PKC target motif (RSTK) or an adjacent serine residue abolish P0 adhesion function and can cause peripheral neuropathy in humans.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP963611.RA9z32HzVIIY0c-Inzf9jpPRipvLcKmB5JIuBQPPM8mZE130_provenance.
- NP963611.RA9z32HzVIIY0c-Inzf9jpPRipvLcKmB5JIuBQPPM8mZE130_assertion evidence source_evidence_literature NP963611.RA9z32HzVIIY0c-Inzf9jpPRipvLcKmB5JIuBQPPM8mZE130_provenance.
- NP963611.RA9z32HzVIIY0c-Inzf9jpPRipvLcKmB5JIuBQPPM8mZE130_assertion SIO_000772 11673479 NP963611.RA9z32HzVIIY0c-Inzf9jpPRipvLcKmB5JIuBQPPM8mZE130_provenance.
- NP963611.RA9z32HzVIIY0c-Inzf9jpPRipvLcKmB5JIuBQPPM8mZE130_assertion wasDerivedFrom befree-20150227 NP963611.RA9z32HzVIIY0c-Inzf9jpPRipvLcKmB5JIuBQPPM8mZE130_provenance.
- NP963611.RA9z32HzVIIY0c-Inzf9jpPRipvLcKmB5JIuBQPPM8mZE130_assertion wasGeneratedBy ECO_0000203 NP963611.RA9z32HzVIIY0c-Inzf9jpPRipvLcKmB5JIuBQPPM8mZE130_provenance.
- befree-20150227 importedOn "2015-02-27" NP963611.RA9z32HzVIIY0c-Inzf9jpPRipvLcKmB5JIuBQPPM8mZE130_provenance.