Matches in Nanopublications for { <http://rdf.disgenet.org/nanopublications.trig#NP545162.RAuifAf7b4yLHCCWBa6NYdLHHfn4iUXv05_WZNT8egNxc130_assertion> ?p ?o ?g. }
Showing items 1 to 6 of
6
with 100 items per page.
- NP545162.RAuifAf7b4yLHCCWBa6NYdLHHfn4iUXv05_WZNT8egNxc130_assertion type Assertion NP545162.RAuifAf7b4yLHCCWBa6NYdLHHfn4iUXv05_WZNT8egNxc130_head.
- NP545162.RAuifAf7b4yLHCCWBa6NYdLHHfn4iUXv05_WZNT8egNxc130_assertion wasGeneratedBy ECO_0000203 NP545162.RAuifAf7b4yLHCCWBa6NYdLHHfn4iUXv05_WZNT8egNxc130_provenance.
- NP545162.RAuifAf7b4yLHCCWBa6NYdLHHfn4iUXv05_WZNT8egNxc130_assertion wasDerivedFrom befree-20140225 NP545162.RAuifAf7b4yLHCCWBa6NYdLHHfn4iUXv05_WZNT8egNxc130_provenance.
- NP545162.RAuifAf7b4yLHCCWBa6NYdLHHfn4iUXv05_WZNT8egNxc130_assertion SIO_000772 17855451 NP545162.RAuifAf7b4yLHCCWBa6NYdLHHfn4iUXv05_WZNT8egNxc130_provenance.
- NP545162.RAuifAf7b4yLHCCWBa6NYdLHHfn4iUXv05_WZNT8egNxc130_assertion evidence source_evidence_literature NP545162.RAuifAf7b4yLHCCWBa6NYdLHHfn4iUXv05_WZNT8egNxc130_provenance.
- NP545162.RAuifAf7b4yLHCCWBa6NYdLHHfn4iUXv05_WZNT8egNxc130_assertion description "[Peripheral demyelinating neuropathy, central dysmyelinating leukodystrophy, Waardenburg syndrome and Hirschsprung disease (PCWH) is a complex neurocristopathy caused by SOX10 mutations.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP545162.RAuifAf7b4yLHCCWBa6NYdLHHfn4iUXv05_WZNT8egNxc130_provenance.