Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP269980.RAG638PYpflYJ4a0s6Su7mY2Cf9iOFp8J9ZLuLP8jBsHY130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP269980.RAG638PYpflYJ4a0s6Su7mY2Cf9iOFp8J9ZLuLP8jBsHY130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP269980.RAG638PYpflYJ4a0s6Su7mY2Cf9iOFp8J9ZLuLP8jBsHY130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP269980.RAG638PYpflYJ4a0s6Su7mY2Cf9iOFp8J9ZLuLP8jBsHY130_provenance.
- befree-20150227 importedOn "2015-02-27" NP269980.RAG638PYpflYJ4a0s6Su7mY2Cf9iOFp8J9ZLuLP8jBsHY130_provenance.
- NP269980.RAG638PYpflYJ4a0s6Su7mY2Cf9iOFp8J9ZLuLP8jBsHY130_assertion wasGeneratedBy ECO_0000203 NP269980.RAG638PYpflYJ4a0s6Su7mY2Cf9iOFp8J9ZLuLP8jBsHY130_provenance.
- NP269980.RAG638PYpflYJ4a0s6Su7mY2Cf9iOFp8J9ZLuLP8jBsHY130_assertion wasDerivedFrom befree-20150227 NP269980.RAG638PYpflYJ4a0s6Su7mY2Cf9iOFp8J9ZLuLP8jBsHY130_provenance.
- NP269980.RAG638PYpflYJ4a0s6Su7mY2Cf9iOFp8J9ZLuLP8jBsHY130_assertion SIO_000772 22474227 NP269980.RAG638PYpflYJ4a0s6Su7mY2Cf9iOFp8J9ZLuLP8jBsHY130_provenance.
- NP269980.RAG638PYpflYJ4a0s6Su7mY2Cf9iOFp8J9ZLuLP8jBsHY130_assertion evidence source_evidence_literature NP269980.RAG638PYpflYJ4a0s6Su7mY2Cf9iOFp8J9ZLuLP8jBsHY130_provenance.
- NP269980.RAG638PYpflYJ4a0s6Su7mY2Cf9iOFp8J9ZLuLP8jBsHY130_assertion description "[Heritable and idiopathic pulmonary arterial hypertension (PAH) are phenotypically identical and associated with mutations in several genes related to transforming growth factor (TGF) beta signaling, including bone morphogenetic protein receptor type 2, activin receptor-like kinase 1, endoglin, and mothers against decapentaplegic 9.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP269980.RAG638PYpflYJ4a0s6Su7mY2Cf9iOFp8J9ZLuLP8jBsHY130_provenance.