Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP5248.RA2HaX2npqyWFpE9RK37QX4T-vWYssfXSdPdgyfyLy1Qc130_provenance>. }
Showing items 1 to 9 of
9
with 100 items per page.
- source_evidence_curated type ECO_0000205 NP5248.RA2HaX2npqyWFpE9RK37QX4T-vWYssfXSdPdgyfyLy1Qc130_provenance.
- source_evidence_curated label "DisGeNET evidence - CURATED" NP5248.RA2HaX2npqyWFpE9RK37QX4T-vWYssfXSdPdgyfyLy1Qc130_provenance.
- source_evidence_curated comment "Gene-disease associations manually curated." NP5248.RA2HaX2npqyWFpE9RK37QX4T-vWYssfXSdPdgyfyLy1Qc130_provenance.
- NP5248.RA2HaX2npqyWFpE9RK37QX4T-vWYssfXSdPdgyfyLy1Qc130_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." NP5248.RA2HaX2npqyWFpE9RK37QX4T-vWYssfXSdPdgyfyLy1Qc130_provenance.
- NP5248.RA2HaX2npqyWFpE9RK37QX4T-vWYssfXSdPdgyfyLy1Qc130_assertion evidence source_evidence_curated NP5248.RA2HaX2npqyWFpE9RK37QX4T-vWYssfXSdPdgyfyLy1Qc130_provenance.
- NP5248.RA2HaX2npqyWFpE9RK37QX4T-vWYssfXSdPdgyfyLy1Qc130_assertion SIO_000772 2475424 NP5248.RA2HaX2npqyWFpE9RK37QX4T-vWYssfXSdPdgyfyLy1Qc130_provenance.
- NP5248.RA2HaX2npqyWFpE9RK37QX4T-vWYssfXSdPdgyfyLy1Qc130_assertion wasDerivedFrom ctd_human-20150221 NP5248.RA2HaX2npqyWFpE9RK37QX4T-vWYssfXSdPdgyfyLy1Qc130_provenance.
- NP5248.RA2HaX2npqyWFpE9RK37QX4T-vWYssfXSdPdgyfyLy1Qc130_assertion wasGeneratedBy ECO_0000218 NP5248.RA2HaX2npqyWFpE9RK37QX4T-vWYssfXSdPdgyfyLy1Qc130_provenance.
- ctd_human-20150221 importedOn "2015-02-21" NP5248.RA2HaX2npqyWFpE9RK37QX4T-vWYssfXSdPdgyfyLy1Qc130_provenance.