Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP825749.RAEp7brbNCgaRBy-KY5EQ6aHTeWDSV1fwB66KTmZ_bnSQ130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP825749.RAEp7brbNCgaRBy-KY5EQ6aHTeWDSV1fwB66KTmZ_bnSQ130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP825749.RAEp7brbNCgaRBy-KY5EQ6aHTeWDSV1fwB66KTmZ_bnSQ130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP825749.RAEp7brbNCgaRBy-KY5EQ6aHTeWDSV1fwB66KTmZ_bnSQ130_provenance.
- NP825749.RAEp7brbNCgaRBy-KY5EQ6aHTeWDSV1fwB66KTmZ_bnSQ130_assertion description "[We have mapped this gene to the 3 Mb critical region of gene loss of the 5q- syndrome within 5q32, flanked by the genes for ADRB2 and IL12B, using gene dosage analysis.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP825749.RAEp7brbNCgaRBy-KY5EQ6aHTeWDSV1fwB66KTmZ_bnSQ130_provenance.
- NP825749.RAEp7brbNCgaRBy-KY5EQ6aHTeWDSV1fwB66KTmZ_bnSQ130_assertion evidence source_evidence_literature NP825749.RAEp7brbNCgaRBy-KY5EQ6aHTeWDSV1fwB66KTmZ_bnSQ130_provenance.
- NP825749.RAEp7brbNCgaRBy-KY5EQ6aHTeWDSV1fwB66KTmZ_bnSQ130_assertion SIO_000772 10982193 NP825749.RAEp7brbNCgaRBy-KY5EQ6aHTeWDSV1fwB66KTmZ_bnSQ130_provenance.
- NP825749.RAEp7brbNCgaRBy-KY5EQ6aHTeWDSV1fwB66KTmZ_bnSQ130_assertion wasDerivedFrom befree-20140225 NP825749.RAEp7brbNCgaRBy-KY5EQ6aHTeWDSV1fwB66KTmZ_bnSQ130_provenance.
- NP825749.RAEp7brbNCgaRBy-KY5EQ6aHTeWDSV1fwB66KTmZ_bnSQ130_assertion wasGeneratedBy ECO_0000203 NP825749.RAEp7brbNCgaRBy-KY5EQ6aHTeWDSV1fwB66KTmZ_bnSQ130_provenance.
- befree-20140225 importedOn "2014-02-25" NP825749.RAEp7brbNCgaRBy-KY5EQ6aHTeWDSV1fwB66KTmZ_bnSQ130_provenance.