Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP905516.RAwjWALyU5SjTx920d5k5d41r0ccdd1XyXk69l3tc8m8M130_provenance>. }
Showing items 1 to 9 of
9
with 100 items per page.
- source_evidence_literature type ECO_0000212 NP905516.RAwjWALyU5SjTx920d5k5d41r0ccdd1XyXk69l3tc8m8M130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP905516.RAwjWALyU5SjTx920d5k5d41r0ccdd1XyXk69l3tc8m8M130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP905516.RAwjWALyU5SjTx920d5k5d41r0ccdd1XyXk69l3tc8m8M130_provenance.
- NP905516.RAwjWALyU5SjTx920d5k5d41r0ccdd1XyXk69l3tc8m8M130_assertion wasGeneratedBy ECO_0000203 NP905516.RAwjWALyU5SjTx920d5k5d41r0ccdd1XyXk69l3tc8m8M130_provenance.
- NP905516.RAwjWALyU5SjTx920d5k5d41r0ccdd1XyXk69l3tc8m8M130_assertion wasDerivedFrom befree-20140225 NP905516.RAwjWALyU5SjTx920d5k5d41r0ccdd1XyXk69l3tc8m8M130_provenance.
- NP905516.RAwjWALyU5SjTx920d5k5d41r0ccdd1XyXk69l3tc8m8M130_assertion SIO_000772 12107438 NP905516.RAwjWALyU5SjTx920d5k5d41r0ccdd1XyXk69l3tc8m8M130_provenance.
- NP905516.RAwjWALyU5SjTx920d5k5d41r0ccdd1XyXk69l3tc8m8M130_assertion evidence source_evidence_literature NP905516.RAwjWALyU5SjTx920d5k5d41r0ccdd1XyXk69l3tc8m8M130_provenance.
- NP905516.RAwjWALyU5SjTx920d5k5d41r0ccdd1XyXk69l3tc8m8M130_assertion description "[We found an IVS12+5G-->C mutation in the USHIC gene, which is associated with nonsyndromic recessive deafness ( DFNB18) segregating in the original family, S-11/12.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP905516.RAwjWALyU5SjTx920d5k5d41r0ccdd1XyXk69l3tc8m8M130_provenance.
- befree-20140225 importedOn "2014-02-25" NP905516.RAwjWALyU5SjTx920d5k5d41r0ccdd1XyXk69l3tc8m8M130_provenance.