Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP5248.RA2HaX2npqyWFpE9RK37QX4T-vWYssfXSdPdgyfyLy1Qc130_assertion> ?p ?o ?g. }
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- NP5248.RA2HaX2npqyWFpE9RK37QX4T-vWYssfXSdPdgyfyLy1Qc130_assertion type Assertion NP5248.RA2HaX2npqyWFpE9RK37QX4T-vWYssfXSdPdgyfyLy1Qc130_head.
- 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.