Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP677032.RA27irjQtdHRulXX_ROLbv678BQaty7sAaX25qMQcYrOU130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP677032.RA27irjQtdHRulXX_ROLbv678BQaty7sAaX25qMQcYrOU130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP677032.RA27irjQtdHRulXX_ROLbv678BQaty7sAaX25qMQcYrOU130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP677032.RA27irjQtdHRulXX_ROLbv678BQaty7sAaX25qMQcYrOU130_provenance.
- NP677032.RA27irjQtdHRulXX_ROLbv678BQaty7sAaX25qMQcYrOU130_assertion description "[We found that point mutations in the coding region of DMRT1 and the DM domain of DMRT2 are not frequent in XY females.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP677032.RA27irjQtdHRulXX_ROLbv678BQaty7sAaX25qMQcYrOU130_provenance.
- NP677032.RA27irjQtdHRulXX_ROLbv678BQaty7sAaX25qMQcYrOU130_assertion evidence source_evidence_literature NP677032.RA27irjQtdHRulXX_ROLbv678BQaty7sAaX25qMQcYrOU130_provenance.
- NP677032.RA27irjQtdHRulXX_ROLbv678BQaty7sAaX25qMQcYrOU130_assertion SIO_000772 10332030 NP677032.RA27irjQtdHRulXX_ROLbv678BQaty7sAaX25qMQcYrOU130_provenance.
- NP677032.RA27irjQtdHRulXX_ROLbv678BQaty7sAaX25qMQcYrOU130_assertion wasDerivedFrom befree-20140225 NP677032.RA27irjQtdHRulXX_ROLbv678BQaty7sAaX25qMQcYrOU130_provenance.
- NP677032.RA27irjQtdHRulXX_ROLbv678BQaty7sAaX25qMQcYrOU130_assertion wasGeneratedBy ECO_0000203 NP677032.RA27irjQtdHRulXX_ROLbv678BQaty7sAaX25qMQcYrOU130_provenance.
- befree-20140225 importedOn "2014-02-25" NP677032.RA27irjQtdHRulXX_ROLbv678BQaty7sAaX25qMQcYrOU130_provenance.