Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP380636.RA41XRtz1e1bE97TTentFNpEsSC8sCB5h7AqQS0x0kVPM130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP380636.RA41XRtz1e1bE97TTentFNpEsSC8sCB5h7AqQS0x0kVPM130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP380636.RA41XRtz1e1bE97TTentFNpEsSC8sCB5h7AqQS0x0kVPM130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP380636.RA41XRtz1e1bE97TTentFNpEsSC8sCB5h7AqQS0x0kVPM130_provenance.
- NP380636.RA41XRtz1e1bE97TTentFNpEsSC8sCB5h7AqQS0x0kVPM130_assertion description "[Haploinsufficiency of Tbx1 is likely a major determinant of cardiac and craniofacial birth defects associated with DiGeorge syndrome.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP380636.RA41XRtz1e1bE97TTentFNpEsSC8sCB5h7AqQS0x0kVPM130_provenance.
- NP380636.RA41XRtz1e1bE97TTentFNpEsSC8sCB5h7AqQS0x0kVPM130_assertion evidence source_evidence_literature NP380636.RA41XRtz1e1bE97TTentFNpEsSC8sCB5h7AqQS0x0kVPM130_provenance.
- NP380636.RA41XRtz1e1bE97TTentFNpEsSC8sCB5h7AqQS0x0kVPM130_assertion SIO_000772 12533514 NP380636.RA41XRtz1e1bE97TTentFNpEsSC8sCB5h7AqQS0x0kVPM130_provenance.
- NP380636.RA41XRtz1e1bE97TTentFNpEsSC8sCB5h7AqQS0x0kVPM130_assertion wasDerivedFrom befree-2016 NP380636.RA41XRtz1e1bE97TTentFNpEsSC8sCB5h7AqQS0x0kVPM130_provenance.
- NP380636.RA41XRtz1e1bE97TTentFNpEsSC8sCB5h7AqQS0x0kVPM130_assertion wasGeneratedBy ECO_0000203 NP380636.RA41XRtz1e1bE97TTentFNpEsSC8sCB5h7AqQS0x0kVPM130_provenance.
- befree-2016 importedOn "2016-02-19" NP380636.RA41XRtz1e1bE97TTentFNpEsSC8sCB5h7AqQS0x0kVPM130_provenance.