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- source_evidence_literature type ECO_0000212 NP216787.RA5PINCTi-sUEgyuG5FdTpJRsa1K_0WzOBITY3vyOSY9I130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP216787.RA5PINCTi-sUEgyuG5FdTpJRsa1K_0WzOBITY3vyOSY9I130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP216787.RA5PINCTi-sUEgyuG5FdTpJRsa1K_0WzOBITY3vyOSY9I130_provenance.
- NP216787.RA5PINCTi-sUEgyuG5FdTpJRsa1K_0WzOBITY3vyOSY9I130_assertion description "[Mutational analysis of the RSPO1 gene in a 46, XX woman with true hermaphroditism, palmoplantar keratoderma, congenital bilateral corneal opacities, onychodystrophy, and hearing impairment, is reported.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP216787.RA5PINCTi-sUEgyuG5FdTpJRsa1K_0WzOBITY3vyOSY9I130_provenance.
- NP216787.RA5PINCTi-sUEgyuG5FdTpJRsa1K_0WzOBITY3vyOSY9I130_assertion evidence source_evidence_literature NP216787.RA5PINCTi-sUEgyuG5FdTpJRsa1K_0WzOBITY3vyOSY9I130_provenance.
- NP216787.RA5PINCTi-sUEgyuG5FdTpJRsa1K_0WzOBITY3vyOSY9I130_assertion SIO_000772 18085567 NP216787.RA5PINCTi-sUEgyuG5FdTpJRsa1K_0WzOBITY3vyOSY9I130_provenance.
- NP216787.RA5PINCTi-sUEgyuG5FdTpJRsa1K_0WzOBITY3vyOSY9I130_assertion wasDerivedFrom lhgdn-20090331 NP216787.RA5PINCTi-sUEgyuG5FdTpJRsa1K_0WzOBITY3vyOSY9I130_provenance.
- NP216787.RA5PINCTi-sUEgyuG5FdTpJRsa1K_0WzOBITY3vyOSY9I130_assertion wasGeneratedBy ECO_0000203 NP216787.RA5PINCTi-sUEgyuG5FdTpJRsa1K_0WzOBITY3vyOSY9I130_provenance.
- lhgdn-20090331 importedOn "2009-03-31" NP216787.RA5PINCTi-sUEgyuG5FdTpJRsa1K_0WzOBITY3vyOSY9I130_provenance.