Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP505175.RAK1OX28Evs_34CgnuwxuTX2yfl_0lZDy4BMZlayt62pg130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP505175.RAK1OX28Evs_34CgnuwxuTX2yfl_0lZDy4BMZlayt62pg130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP505175.RAK1OX28Evs_34CgnuwxuTX2yfl_0lZDy4BMZlayt62pg130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP505175.RAK1OX28Evs_34CgnuwxuTX2yfl_0lZDy4BMZlayt62pg130_provenance.
- NP505175.RAK1OX28Evs_34CgnuwxuTX2yfl_0lZDy4BMZlayt62pg130_assertion description "[We report on two related individuals who have multiple anomalies with parietal foramina and the deletion of 11(p11.12p12) due to the inheritance of a derivative chromosome 11 from an insertional translocation dir ins (13;11)(q14.1; p11.12p12).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP505175.RAK1OX28Evs_34CgnuwxuTX2yfl_0lZDy4BMZlayt62pg130_provenance.
- NP505175.RAK1OX28Evs_34CgnuwxuTX2yfl_0lZDy4BMZlayt62pg130_assertion evidence source_evidence_literature NP505175.RAK1OX28Evs_34CgnuwxuTX2yfl_0lZDy4BMZlayt62pg130_provenance.
- NP505175.RAK1OX28Evs_34CgnuwxuTX2yfl_0lZDy4BMZlayt62pg130_assertion SIO_000772 8456828 NP505175.RAK1OX28Evs_34CgnuwxuTX2yfl_0lZDy4BMZlayt62pg130_provenance.
- NP505175.RAK1OX28Evs_34CgnuwxuTX2yfl_0lZDy4BMZlayt62pg130_assertion wasDerivedFrom befree-20140225 NP505175.RAK1OX28Evs_34CgnuwxuTX2yfl_0lZDy4BMZlayt62pg130_provenance.
- NP505175.RAK1OX28Evs_34CgnuwxuTX2yfl_0lZDy4BMZlayt62pg130_assertion wasGeneratedBy ECO_0000203 NP505175.RAK1OX28Evs_34CgnuwxuTX2yfl_0lZDy4BMZlayt62pg130_provenance.
- befree-20140225 importedOn "2014-02-25" NP505175.RAK1OX28Evs_34CgnuwxuTX2yfl_0lZDy4BMZlayt62pg130_provenance.