5469071

Source:http://linkedlifedata.com/resource/pubmed/id/5469071

Download in:

Switch to

Custom View

Named Graph Language Inference

Statements in which the resource exists as a subject.
Predicate	Object
rdf:type	pubmed:Citation
lifeskim:mentions	umls-concept:C0221757, umls-concept:C0439660, umls-concept:C0600260
pubmed:issue	2
pubmed:dateCreated	1970-11-6
pubmed:language	eng
pubmed:journal	http://linkedlifedata.com/resource/pubmed/journal/7501160
pubmed:citationSubset	AIM
pubmed:chemical	http://linkedlifedata.com/resource/pubmed/chemical/Serum Albumin, http://linkedlifedata.com/resource/pubmed/chemical/Trypsin Inhibitors
pubmed:status	MEDLINE
pubmed:month	Oct
pubmed:issn	0098-7484
pubmed:author	pubmed-author:BrodyA WAW, pubmed-author:LynchHH, pubmed-author:RyningFF, pubmed-author:TownleyR GRG
pubmed:issnType	Print
pubmed:day	12
pubmed:volume	214
pubmed:owner	NLM
pubmed:authorsComplete	Y
pubmed:pagination	325-31
pubmed:dateRevised	2006-11-7
pubmed:meshHeading	pubmed-meshheading:5469071-Adolescent, pubmed-meshheading:5469071-Adult, pubmed-meshheading:5469071-Age Factors, pubmed-meshheading:5469071-Anoxia, pubmed-meshheading:5469071-Asthma, pubmed-meshheading:5469071-Blood Protein Electrophoresis, pubmed-meshheading:5469071-Child, pubmed-meshheading:5469071-Diagnosis, Differential, pubmed-meshheading:5469071-Dyspnea, Paroxysmal, pubmed-meshheading:5469071-Female, pubmed-meshheading:5469071-Heterozygote, pubmed-meshheading:5469071-Homozygote, pubmed-meshheading:5469071-Humans, pubmed-meshheading:5469071-Immunoelectrophoresis, pubmed-meshheading:5469071-Lung Compliance, pubmed-meshheading:5469071-Male, pubmed-meshheading:5469071-Metabolism, Inborn Errors, pubmed-meshheading:5469071-Middle Aged, pubmed-meshheading:5469071-Pedigree, pubmed-meshheading:5469071-Pulmonary Emphysema, pubmed-meshheading:5469071-Respiratory Insufficiency, pubmed-meshheading:5469071-Serum Albumin, pubmed-meshheading:5469071-Trypsin Inhibitors, pubmed-meshheading:5469071-Vital Capacity
pubmed:year	1970
pubmed:articleTitle	Obstructive lung disease in hereditary alpha 1-antitrypsin deficiency.
pubmed:publicationType	Journal Article