Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP96096.RAzl0g7zkwOtMOg3MXxtm2l3rGNXnuKOsXLFSW-v-aEpk130_provenance>. }
Showing items 1 to 9 of
9
with 100 items per page.
- source_evidence_literature type ECO_0000212 NP96096.RAzl0g7zkwOtMOg3MXxtm2l3rGNXnuKOsXLFSW-v-aEpk130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP96096.RAzl0g7zkwOtMOg3MXxtm2l3rGNXnuKOsXLFSW-v-aEpk130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP96096.RAzl0g7zkwOtMOg3MXxtm2l3rGNXnuKOsXLFSW-v-aEpk130_provenance.
- NP96096.RAzl0g7zkwOtMOg3MXxtm2l3rGNXnuKOsXLFSW-v-aEpk130_assertion description "[These results provide genetic basis for gender differences in MDD and will serve as a resource for replication in other populations to elucidate the potential role of these genetic variants in MDD.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP96096.RAzl0g7zkwOtMOg3MXxtm2l3rGNXnuKOsXLFSW-v-aEpk130_provenance.
- NP96096.RAzl0g7zkwOtMOg3MXxtm2l3rGNXnuKOsXLFSW-v-aEpk130_assertion evidence source_evidence_literature NP96096.RAzl0g7zkwOtMOg3MXxtm2l3rGNXnuKOsXLFSW-v-aEpk130_provenance.
- NP96096.RAzl0g7zkwOtMOg3MXxtm2l3rGNXnuKOsXLFSW-v-aEpk130_assertion SIO_000772 21621269 NP96096.RAzl0g7zkwOtMOg3MXxtm2l3rGNXnuKOsXLFSW-v-aEpk130_provenance.
- NP96096.RAzl0g7zkwOtMOg3MXxtm2l3rGNXnuKOsXLFSW-v-aEpk130_assertion wasDerivedFrom gad-20130706 NP96096.RAzl0g7zkwOtMOg3MXxtm2l3rGNXnuKOsXLFSW-v-aEpk130_provenance.
- NP96096.RAzl0g7zkwOtMOg3MXxtm2l3rGNXnuKOsXLFSW-v-aEpk130_assertion wasGeneratedBy ECO_0000203 NP96096.RAzl0g7zkwOtMOg3MXxtm2l3rGNXnuKOsXLFSW-v-aEpk130_provenance.
- gad-20130706 importedOn "2013-07-06" NP96096.RAzl0g7zkwOtMOg3MXxtm2l3rGNXnuKOsXLFSW-v-aEpk130_provenance.