Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP663216.RAmelHLQqy_50t30cx49ZXnJ4L8xYTWIkPi-aTcdXpXvU130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP663216.RAmelHLQqy_50t30cx49ZXnJ4L8xYTWIkPi-aTcdXpXvU130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP663216.RAmelHLQqy_50t30cx49ZXnJ4L8xYTWIkPi-aTcdXpXvU130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP663216.RAmelHLQqy_50t30cx49ZXnJ4L8xYTWIkPi-aTcdXpXvU130_provenance.
- NP663216.RAmelHLQqy_50t30cx49ZXnJ4L8xYTWIkPi-aTcdXpXvU130_assertion description "[Diverse heterozygous mutations of bone morphogenetic receptor type II (BMPR-II) underlie the inherited form of the vascular disorder primary pulmonary hypertension (PPH).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP663216.RAmelHLQqy_50t30cx49ZXnJ4L8xYTWIkPi-aTcdXpXvU130_provenance.
- NP663216.RAmelHLQqy_50t30cx49ZXnJ4L8xYTWIkPi-aTcdXpXvU130_assertion evidence source_evidence_literature NP663216.RAmelHLQqy_50t30cx49ZXnJ4L8xYTWIkPi-aTcdXpXvU130_provenance.
- NP663216.RAmelHLQqy_50t30cx49ZXnJ4L8xYTWIkPi-aTcdXpXvU130_assertion SIO_000772 14583445 NP663216.RAmelHLQqy_50t30cx49ZXnJ4L8xYTWIkPi-aTcdXpXvU130_provenance.
- NP663216.RAmelHLQqy_50t30cx49ZXnJ4L8xYTWIkPi-aTcdXpXvU130_assertion wasDerivedFrom befree-20140225 NP663216.RAmelHLQqy_50t30cx49ZXnJ4L8xYTWIkPi-aTcdXpXvU130_provenance.
- NP663216.RAmelHLQqy_50t30cx49ZXnJ4L8xYTWIkPi-aTcdXpXvU130_assertion wasGeneratedBy ECO_0000203 NP663216.RAmelHLQqy_50t30cx49ZXnJ4L8xYTWIkPi-aTcdXpXvU130_provenance.
- befree-20140225 importedOn "2014-02-25" NP663216.RAmelHLQqy_50t30cx49ZXnJ4L8xYTWIkPi-aTcdXpXvU130_provenance.