Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP889184.RAL9t7PE36IvLJm1Sdsc70k1gXUFBRi-xm5JTiLrtph20130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP889184.RAL9t7PE36IvLJm1Sdsc70k1gXUFBRi-xm5JTiLrtph20130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP889184.RAL9t7PE36IvLJm1Sdsc70k1gXUFBRi-xm5JTiLrtph20130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP889184.RAL9t7PE36IvLJm1Sdsc70k1gXUFBRi-xm5JTiLrtph20130_provenance.
- NP889184.RAL9t7PE36IvLJm1Sdsc70k1gXUFBRi-xm5JTiLrtph20130_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." NP889184.RAL9t7PE36IvLJm1Sdsc70k1gXUFBRi-xm5JTiLrtph20130_provenance.
- NP889184.RAL9t7PE36IvLJm1Sdsc70k1gXUFBRi-xm5JTiLrtph20130_assertion evidence source_evidence_literature NP889184.RAL9t7PE36IvLJm1Sdsc70k1gXUFBRi-xm5JTiLrtph20130_provenance.
- NP889184.RAL9t7PE36IvLJm1Sdsc70k1gXUFBRi-xm5JTiLrtph20130_assertion SIO_000772 10493923 NP889184.RAL9t7PE36IvLJm1Sdsc70k1gXUFBRi-xm5JTiLrtph20130_provenance.
- NP889184.RAL9t7PE36IvLJm1Sdsc70k1gXUFBRi-xm5JTiLrtph20130_assertion wasDerivedFrom befree-20140225 NP889184.RAL9t7PE36IvLJm1Sdsc70k1gXUFBRi-xm5JTiLrtph20130_provenance.
- NP889184.RAL9t7PE36IvLJm1Sdsc70k1gXUFBRi-xm5JTiLrtph20130_assertion wasGeneratedBy ECO_0000203 NP889184.RAL9t7PE36IvLJm1Sdsc70k1gXUFBRi-xm5JTiLrtph20130_provenance.
- befree-20140225 importedOn "2014-02-25" NP889184.RAL9t7PE36IvLJm1Sdsc70k1gXUFBRi-xm5JTiLrtph20130_provenance.