Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP92102.RAmUDQ_3y9Lyu7CwaqmvpxdhQxmvLyVadn1sNAuJPsy50130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP92102.RAmUDQ_3y9Lyu7CwaqmvpxdhQxmvLyVadn1sNAuJPsy50130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP92102.RAmUDQ_3y9Lyu7CwaqmvpxdhQxmvLyVadn1sNAuJPsy50130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP92102.RAmUDQ_3y9Lyu7CwaqmvpxdhQxmvLyVadn1sNAuJPsy50130_provenance.
- NP92102.RAmUDQ_3y9Lyu7CwaqmvpxdhQxmvLyVadn1sNAuJPsy50130_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." NP92102.RAmUDQ_3y9Lyu7CwaqmvpxdhQxmvLyVadn1sNAuJPsy50130_provenance.
- NP92102.RAmUDQ_3y9Lyu7CwaqmvpxdhQxmvLyVadn1sNAuJPsy50130_assertion evidence source_evidence_literature NP92102.RAmUDQ_3y9Lyu7CwaqmvpxdhQxmvLyVadn1sNAuJPsy50130_provenance.
- NP92102.RAmUDQ_3y9Lyu7CwaqmvpxdhQxmvLyVadn1sNAuJPsy50130_assertion SIO_000772 15846854 NP92102.RAmUDQ_3y9Lyu7CwaqmvpxdhQxmvLyVadn1sNAuJPsy50130_provenance.
- NP92102.RAmUDQ_3y9Lyu7CwaqmvpxdhQxmvLyVadn1sNAuJPsy50130_assertion wasDerivedFrom gad-20150221 NP92102.RAmUDQ_3y9Lyu7CwaqmvpxdhQxmvLyVadn1sNAuJPsy50130_provenance.
- NP92102.RAmUDQ_3y9Lyu7CwaqmvpxdhQxmvLyVadn1sNAuJPsy50130_assertion wasGeneratedBy ECO_0000203 NP92102.RAmUDQ_3y9Lyu7CwaqmvpxdhQxmvLyVadn1sNAuJPsy50130_provenance.
- gad-20150221 importedOn "2015-02-21" NP92102.RAmUDQ_3y9Lyu7CwaqmvpxdhQxmvLyVadn1sNAuJPsy50130_provenance.