Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP143436.RAdbCYEubMi_ESDeIoBLSdinTNoEynis1m1_MUUuQDcmM130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP143436.RAdbCYEubMi_ESDeIoBLSdinTNoEynis1m1_MUUuQDcmM130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP143436.RAdbCYEubMi_ESDeIoBLSdinTNoEynis1m1_MUUuQDcmM130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP143436.RAdbCYEubMi_ESDeIoBLSdinTNoEynis1m1_MUUuQDcmM130_provenance.
- NP143436.RAdbCYEubMi_ESDeIoBLSdinTNoEynis1m1_MUUuQDcmM130_assertion description "[However, we identified rare variants in ENG and TGFBR3 that may be important for IA pathogenesis in a subset of families.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP143436.RAdbCYEubMi_ESDeIoBLSdinTNoEynis1m1_MUUuQDcmM130_provenance.
- NP143436.RAdbCYEubMi_ESDeIoBLSdinTNoEynis1m1_MUUuQDcmM130_assertion evidence source_evidence_literature NP143436.RAdbCYEubMi_ESDeIoBLSdinTNoEynis1m1_MUUuQDcmM130_provenance.
- NP143436.RAdbCYEubMi_ESDeIoBLSdinTNoEynis1m1_MUUuQDcmM130_assertion SIO_000772 19299629 NP143436.RAdbCYEubMi_ESDeIoBLSdinTNoEynis1m1_MUUuQDcmM130_provenance.
- NP143436.RAdbCYEubMi_ESDeIoBLSdinTNoEynis1m1_MUUuQDcmM130_assertion wasDerivedFrom gad-20150221 NP143436.RAdbCYEubMi_ESDeIoBLSdinTNoEynis1m1_MUUuQDcmM130_provenance.
- NP143436.RAdbCYEubMi_ESDeIoBLSdinTNoEynis1m1_MUUuQDcmM130_assertion wasGeneratedBy ECO_0000203 NP143436.RAdbCYEubMi_ESDeIoBLSdinTNoEynis1m1_MUUuQDcmM130_provenance.
- gad-20150221 importedOn "2015-02-21" NP143436.RAdbCYEubMi_ESDeIoBLSdinTNoEynis1m1_MUUuQDcmM130_provenance.