Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP263644.RAtqBwX7E1IIjwUHintQuD9ZzrqU6-xnRNCwY3inz_RSg130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP263644.RAtqBwX7E1IIjwUHintQuD9ZzrqU6-xnRNCwY3inz_RSg130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP263644.RAtqBwX7E1IIjwUHintQuD9ZzrqU6-xnRNCwY3inz_RSg130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP263644.RAtqBwX7E1IIjwUHintQuD9ZzrqU6-xnRNCwY3inz_RSg130_provenance.
- NP263644.RAtqBwX7E1IIjwUHintQuD9ZzrqU6-xnRNCwY3inz_RSg130_assertion description "[Although the relative abundance of the deletion form of SP-B mRNA remains constant among normal lungs, it is found with relatively higher abundance in the lungs of some individuals with diseases such as congenital alveolar proteinosis, respiratory distress syndrome, bronchopulmonary dysplasia, alveolar capillary dysplasia and hypophosphatasia.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP263644.RAtqBwX7E1IIjwUHintQuD9ZzrqU6-xnRNCwY3inz_RSg130_provenance.
- NP263644.RAtqBwX7E1IIjwUHintQuD9ZzrqU6-xnRNCwY3inz_RSg130_assertion evidence source_evidence_literature NP263644.RAtqBwX7E1IIjwUHintQuD9ZzrqU6-xnRNCwY3inz_RSg130_provenance.
- NP263644.RAtqBwX7E1IIjwUHintQuD9ZzrqU6-xnRNCwY3inz_RSg130_assertion SIO_000772 10493923 NP263644.RAtqBwX7E1IIjwUHintQuD9ZzrqU6-xnRNCwY3inz_RSg130_provenance.
- NP263644.RAtqBwX7E1IIjwUHintQuD9ZzrqU6-xnRNCwY3inz_RSg130_assertion wasDerivedFrom befree-2016 NP263644.RAtqBwX7E1IIjwUHintQuD9ZzrqU6-xnRNCwY3inz_RSg130_provenance.
- NP263644.RAtqBwX7E1IIjwUHintQuD9ZzrqU6-xnRNCwY3inz_RSg130_assertion wasGeneratedBy ECO_0000203 NP263644.RAtqBwX7E1IIjwUHintQuD9ZzrqU6-xnRNCwY3inz_RSg130_provenance.
- befree-2016 importedOn "2016-02-19" NP263644.RAtqBwX7E1IIjwUHintQuD9ZzrqU6-xnRNCwY3inz_RSg130_provenance.