Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP62167.RA1XZQaqoob2NtfXEuOk9NtHF4xGFX1b3I2sCaS_EpOMU130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP62167.RA1XZQaqoob2NtfXEuOk9NtHF4xGFX1b3I2sCaS_EpOMU130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP62167.RA1XZQaqoob2NtfXEuOk9NtHF4xGFX1b3I2sCaS_EpOMU130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP62167.RA1XZQaqoob2NtfXEuOk9NtHF4xGFX1b3I2sCaS_EpOMU130_provenance.
- NP62167.RA1XZQaqoob2NtfXEuOk9NtHF4xGFX1b3I2sCaS_EpOMU130_assertion description "[A significant difference in one haplotype was observed in AD patients without the APOE epsilon4 allele.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP62167.RA1XZQaqoob2NtfXEuOk9NtHF4xGFX1b3I2sCaS_EpOMU130_provenance.
- NP62167.RA1XZQaqoob2NtfXEuOk9NtHF4xGFX1b3I2sCaS_EpOMU130_assertion evidence source_evidence_literature NP62167.RA1XZQaqoob2NtfXEuOk9NtHF4xGFX1b3I2sCaS_EpOMU130_provenance.
- NP62167.RA1XZQaqoob2NtfXEuOk9NtHF4xGFX1b3I2sCaS_EpOMU130_assertion SIO_000772 15249634 NP62167.RA1XZQaqoob2NtfXEuOk9NtHF4xGFX1b3I2sCaS_EpOMU130_provenance.
- NP62167.RA1XZQaqoob2NtfXEuOk9NtHF4xGFX1b3I2sCaS_EpOMU130_assertion wasDerivedFrom gad-20130706 NP62167.RA1XZQaqoob2NtfXEuOk9NtHF4xGFX1b3I2sCaS_EpOMU130_provenance.
- NP62167.RA1XZQaqoob2NtfXEuOk9NtHF4xGFX1b3I2sCaS_EpOMU130_assertion wasGeneratedBy ECO_0000203 NP62167.RA1XZQaqoob2NtfXEuOk9NtHF4xGFX1b3I2sCaS_EpOMU130_provenance.
- gad-20130706 importedOn "2013-07-06" NP62167.RA1XZQaqoob2NtfXEuOk9NtHF4xGFX1b3I2sCaS_EpOMU130_provenance.