Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP907818.RAInwNPgLqKCiEKL7vRxoNV3K7emIyVJR05jD57YhWrIY130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP907818.RAInwNPgLqKCiEKL7vRxoNV3K7emIyVJR05jD57YhWrIY130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP907818.RAInwNPgLqKCiEKL7vRxoNV3K7emIyVJR05jD57YhWrIY130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP907818.RAInwNPgLqKCiEKL7vRxoNV3K7emIyVJR05jD57YhWrIY130_provenance.
- NP907818.RAInwNPgLqKCiEKL7vRxoNV3K7emIyVJR05jD57YhWrIY130_assertion description "[290 idiopathic (I)PAH patients and 15 heritable (H)PAH were screened to determine the spectrum and rate of BMPR2 mutations in a large Chinese patient group.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP907818.RAInwNPgLqKCiEKL7vRxoNV3K7emIyVJR05jD57YhWrIY130_provenance.
- NP907818.RAInwNPgLqKCiEKL7vRxoNV3K7emIyVJR05jD57YhWrIY130_assertion evidence source_evidence_literature NP907818.RAInwNPgLqKCiEKL7vRxoNV3K7emIyVJR05jD57YhWrIY130_provenance.
- NP907818.RAInwNPgLqKCiEKL7vRxoNV3K7emIyVJR05jD57YhWrIY130_assertion SIO_000772 21737554 NP907818.RAInwNPgLqKCiEKL7vRxoNV3K7emIyVJR05jD57YhWrIY130_provenance.
- NP907818.RAInwNPgLqKCiEKL7vRxoNV3K7emIyVJR05jD57YhWrIY130_assertion wasDerivedFrom befree-2016 NP907818.RAInwNPgLqKCiEKL7vRxoNV3K7emIyVJR05jD57YhWrIY130_provenance.
- NP907818.RAInwNPgLqKCiEKL7vRxoNV3K7emIyVJR05jD57YhWrIY130_assertion wasGeneratedBy ECO_0000203 NP907818.RAInwNPgLqKCiEKL7vRxoNV3K7emIyVJR05jD57YhWrIY130_provenance.
- befree-2016 importedOn "2016-02-19" NP907818.RAInwNPgLqKCiEKL7vRxoNV3K7emIyVJR05jD57YhWrIY130_provenance.