Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP500167.RAQHxzOZK-VdmQ_RtW6Se-SsNnyxFf4I7oaTg1p6dcqIo130_assertion> ?p ?o ?g. }
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- NP500167.RAQHxzOZK-VdmQ_RtW6Se-SsNnyxFf4I7oaTg1p6dcqIo130_assertion type Assertion NP500167.RAQHxzOZK-VdmQ_RtW6Se-SsNnyxFf4I7oaTg1p6dcqIo130_head.
- NP500167.RAQHxzOZK-VdmQ_RtW6Se-SsNnyxFf4I7oaTg1p6dcqIo130_assertion description "[SPTLC1 and RAB7 mutation analysis in dominantly inherited and idiopathic sensory neuropathies.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP500167.RAQHxzOZK-VdmQ_RtW6Se-SsNnyxFf4I7oaTg1p6dcqIo130_provenance.
- NP500167.RAQHxzOZK-VdmQ_RtW6Se-SsNnyxFf4I7oaTg1p6dcqIo130_assertion evidence source_evidence_literature NP500167.RAQHxzOZK-VdmQ_RtW6Se-SsNnyxFf4I7oaTg1p6dcqIo130_provenance.
- NP500167.RAQHxzOZK-VdmQ_RtW6Se-SsNnyxFf4I7oaTg1p6dcqIo130_assertion SIO_000772 15965219 NP500167.RAQHxzOZK-VdmQ_RtW6Se-SsNnyxFf4I7oaTg1p6dcqIo130_provenance.
- NP500167.RAQHxzOZK-VdmQ_RtW6Se-SsNnyxFf4I7oaTg1p6dcqIo130_assertion wasDerivedFrom befree-2016 NP500167.RAQHxzOZK-VdmQ_RtW6Se-SsNnyxFf4I7oaTg1p6dcqIo130_provenance.
- NP500167.RAQHxzOZK-VdmQ_RtW6Se-SsNnyxFf4I7oaTg1p6dcqIo130_assertion wasGeneratedBy ECO_0000203 NP500167.RAQHxzOZK-VdmQ_RtW6Se-SsNnyxFf4I7oaTg1p6dcqIo130_provenance.