Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP140541.RARDg8q6CxbjY3JOV_ACRE_2V7lBEVSN1X9j1Cl4pVHPA130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP140541.RARDg8q6CxbjY3JOV_ACRE_2V7lBEVSN1X9j1Cl4pVHPA130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP140541.RARDg8q6CxbjY3JOV_ACRE_2V7lBEVSN1X9j1Cl4pVHPA130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP140541.RARDg8q6CxbjY3JOV_ACRE_2V7lBEVSN1X9j1Cl4pVHPA130_provenance.
- NP140541.RARDg8q6CxbjY3JOV_ACRE_2V7lBEVSN1X9j1Cl4pVHPA130_assertion description "[Modest associations were observed in CITED2, EP300, CREBBP, TFAP2A and CARM1 but not ALX1. However, these modest associations were not statistically significant after correction for multiple comparisons. Searching for potential functional variants and rar]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP140541.RARDg8q6CxbjY3JOV_ACRE_2V7lBEVSN1X9j1Cl4pVHPA130_provenance.
- NP140541.RARDg8q6CxbjY3JOV_ACRE_2V7lBEVSN1X9j1Cl4pVHPA130_assertion evidence source_evidence_literature NP140541.RARDg8q6CxbjY3JOV_ACRE_2V7lBEVSN1X9j1Cl4pVHPA130_provenance.
- NP140541.RARDg8q6CxbjY3JOV_ACRE_2V7lBEVSN1X9j1Cl4pVHPA130_assertion SIO_000772 20932315 NP140541.RARDg8q6CxbjY3JOV_ACRE_2V7lBEVSN1X9j1Cl4pVHPA130_provenance.
- NP140541.RARDg8q6CxbjY3JOV_ACRE_2V7lBEVSN1X9j1Cl4pVHPA130_assertion wasDerivedFrom gad-20150221 NP140541.RARDg8q6CxbjY3JOV_ACRE_2V7lBEVSN1X9j1Cl4pVHPA130_provenance.
- NP140541.RARDg8q6CxbjY3JOV_ACRE_2V7lBEVSN1X9j1Cl4pVHPA130_assertion wasGeneratedBy ECO_0000203 NP140541.RARDg8q6CxbjY3JOV_ACRE_2V7lBEVSN1X9j1Cl4pVHPA130_provenance.
- gad-20150221 importedOn "2015-02-21" NP140541.RARDg8q6CxbjY3JOV_ACRE_2V7lBEVSN1X9j1Cl4pVHPA130_provenance.