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- source_evidence_literature type ECO_0000212 NP491188.RAzgZltQ4uoLyvp03k4KdcHiTNOlyv_I9fAcXLj--WRRY130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP491188.RAzgZltQ4uoLyvp03k4KdcHiTNOlyv_I9fAcXLj--WRRY130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP491188.RAzgZltQ4uoLyvp03k4KdcHiTNOlyv_I9fAcXLj--WRRY130_provenance.
- befree-2016 importedOn "2016-02-19" NP491188.RAzgZltQ4uoLyvp03k4KdcHiTNOlyv_I9fAcXLj--WRRY130_provenance.
- NP491188.RAzgZltQ4uoLyvp03k4KdcHiTNOlyv_I9fAcXLj--WRRY130_assertion wasGeneratedBy ECO_0000203 NP491188.RAzgZltQ4uoLyvp03k4KdcHiTNOlyv_I9fAcXLj--WRRY130_provenance.
- NP491188.RAzgZltQ4uoLyvp03k4KdcHiTNOlyv_I9fAcXLj--WRRY130_assertion wasDerivedFrom befree-2016 NP491188.RAzgZltQ4uoLyvp03k4KdcHiTNOlyv_I9fAcXLj--WRRY130_provenance.
- NP491188.RAzgZltQ4uoLyvp03k4KdcHiTNOlyv_I9fAcXLj--WRRY130_assertion SIO_000772 15846854 NP491188.RAzgZltQ4uoLyvp03k4KdcHiTNOlyv_I9fAcXLj--WRRY130_provenance.
- NP491188.RAzgZltQ4uoLyvp03k4KdcHiTNOlyv_I9fAcXLj--WRRY130_assertion evidence source_evidence_literature NP491188.RAzgZltQ4uoLyvp03k4KdcHiTNOlyv_I9fAcXLj--WRRY130_provenance.
- NP491188.RAzgZltQ4uoLyvp03k4KdcHiTNOlyv_I9fAcXLj--WRRY130_assertion description "[Effects of COMT genotype on behavioral symptomatology in the 22q11.2 Deletion Syndrome.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP491188.RAzgZltQ4uoLyvp03k4KdcHiTNOlyv_I9fAcXLj--WRRY130_provenance.