Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP964143.RA6taXZpQRGmxzaSTjz228cp9UA772EQUsM7S0EhvrTBw130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP964143.RA6taXZpQRGmxzaSTjz228cp9UA772EQUsM7S0EhvrTBw130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP964143.RA6taXZpQRGmxzaSTjz228cp9UA772EQUsM7S0EhvrTBw130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP964143.RA6taXZpQRGmxzaSTjz228cp9UA772EQUsM7S0EhvrTBw130_provenance.
- NP964143.RA6taXZpQRGmxzaSTjz228cp9UA772EQUsM7S0EhvrTBw130_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." NP964143.RA6taXZpQRGmxzaSTjz228cp9UA772EQUsM7S0EhvrTBw130_provenance.
- NP964143.RA6taXZpQRGmxzaSTjz228cp9UA772EQUsM7S0EhvrTBw130_assertion evidence source_evidence_literature NP964143.RA6taXZpQRGmxzaSTjz228cp9UA772EQUsM7S0EhvrTBw130_provenance.
- NP964143.RA6taXZpQRGmxzaSTjz228cp9UA772EQUsM7S0EhvrTBw130_assertion SIO_000772 22374147 NP964143.RA6taXZpQRGmxzaSTjz228cp9UA772EQUsM7S0EhvrTBw130_provenance.
- NP964143.RA6taXZpQRGmxzaSTjz228cp9UA772EQUsM7S0EhvrTBw130_assertion wasDerivedFrom befree-2016 NP964143.RA6taXZpQRGmxzaSTjz228cp9UA772EQUsM7S0EhvrTBw130_provenance.
- NP964143.RA6taXZpQRGmxzaSTjz228cp9UA772EQUsM7S0EhvrTBw130_assertion wasGeneratedBy ECO_0000203 NP964143.RA6taXZpQRGmxzaSTjz228cp9UA772EQUsM7S0EhvrTBw130_provenance.
- befree-2016 importedOn "2016-02-19" NP964143.RA6taXZpQRGmxzaSTjz228cp9UA772EQUsM7S0EhvrTBw130_provenance.