Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP600134.RAJJPNEHV0s0gW__TtZxm6GdHogeuoiNmWMxON9ehRe-s130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP600134.RAJJPNEHV0s0gW__TtZxm6GdHogeuoiNmWMxON9ehRe-s130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP600134.RAJJPNEHV0s0gW__TtZxm6GdHogeuoiNmWMxON9ehRe-s130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP600134.RAJJPNEHV0s0gW__TtZxm6GdHogeuoiNmWMxON9ehRe-s130_provenance.
- NP600134.RAJJPNEHV0s0gW__TtZxm6GdHogeuoiNmWMxON9ehRe-s130_assertion description "[The patient is heterozygous for an alteration in the A2M gene; this may be responsible for his serum A2M deficiency and may be relevant to the early onset of pulmonary disease in his case.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP600134.RAJJPNEHV0s0gW__TtZxm6GdHogeuoiNmWMxON9ehRe-s130_provenance.
- NP600134.RAJJPNEHV0s0gW__TtZxm6GdHogeuoiNmWMxON9ehRe-s130_assertion evidence source_evidence_literature NP600134.RAJJPNEHV0s0gW__TtZxm6GdHogeuoiNmWMxON9ehRe-s130_provenance.
- NP600134.RAJJPNEHV0s0gW__TtZxm6GdHogeuoiNmWMxON9ehRe-s130_assertion SIO_000772 2475424 NP600134.RAJJPNEHV0s0gW__TtZxm6GdHogeuoiNmWMxON9ehRe-s130_provenance.
- NP600134.RAJJPNEHV0s0gW__TtZxm6GdHogeuoiNmWMxON9ehRe-s130_assertion wasDerivedFrom befree-20140225 NP600134.RAJJPNEHV0s0gW__TtZxm6GdHogeuoiNmWMxON9ehRe-s130_provenance.
- NP600134.RAJJPNEHV0s0gW__TtZxm6GdHogeuoiNmWMxON9ehRe-s130_assertion wasGeneratedBy ECO_0000203 NP600134.RAJJPNEHV0s0gW__TtZxm6GdHogeuoiNmWMxON9ehRe-s130_provenance.
- befree-20140225 importedOn "2014-02-25" NP600134.RAJJPNEHV0s0gW__TtZxm6GdHogeuoiNmWMxON9ehRe-s130_provenance.