Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP918887.RAWCxvdnUog6IITM8zY_HLRzs2iTheqPdmL39qgPe_DTs130_provenance>. }
Showing items 1 to 9 of
9
with 100 items per page.
- source_evidence_literature type ECO_0000212 NP918887.RAWCxvdnUog6IITM8zY_HLRzs2iTheqPdmL39qgPe_DTs130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP918887.RAWCxvdnUog6IITM8zY_HLRzs2iTheqPdmL39qgPe_DTs130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP918887.RAWCxvdnUog6IITM8zY_HLRzs2iTheqPdmL39qgPe_DTs130_provenance.
- NP918887.RAWCxvdnUog6IITM8zY_HLRzs2iTheqPdmL39qgPe_DTs130_assertion description "[Mutations in the bone morphogenetic protein receptor type 2 (BMPR2) gene, the activin receptor-like kinase 1 (ALK1) gene, and SMAD8 gene have been reported in heritable pulmonary arterial hypertension (HPAH) and in idiopathic pulmonary arterial hypertension (IPAH).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP918887.RAWCxvdnUog6IITM8zY_HLRzs2iTheqPdmL39qgPe_DTs130_provenance.
- NP918887.RAWCxvdnUog6IITM8zY_HLRzs2iTheqPdmL39qgPe_DTs130_assertion evidence source_evidence_literature NP918887.RAWCxvdnUog6IITM8zY_HLRzs2iTheqPdmL39qgPe_DTs130_provenance.
- NP918887.RAWCxvdnUog6IITM8zY_HLRzs2iTheqPdmL39qgPe_DTs130_assertion SIO_000772 22374147 NP918887.RAWCxvdnUog6IITM8zY_HLRzs2iTheqPdmL39qgPe_DTs130_provenance.
- NP918887.RAWCxvdnUog6IITM8zY_HLRzs2iTheqPdmL39qgPe_DTs130_assertion wasDerivedFrom befree-20140225 NP918887.RAWCxvdnUog6IITM8zY_HLRzs2iTheqPdmL39qgPe_DTs130_provenance.
- NP918887.RAWCxvdnUog6IITM8zY_HLRzs2iTheqPdmL39qgPe_DTs130_assertion wasGeneratedBy ECO_0000203 NP918887.RAWCxvdnUog6IITM8zY_HLRzs2iTheqPdmL39qgPe_DTs130_provenance.
- befree-20140225 importedOn "2014-02-25" NP918887.RAWCxvdnUog6IITM8zY_HLRzs2iTheqPdmL39qgPe_DTs130_provenance.