Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP548291.RA4x3chV27iPgCh0V4uUhLW3_hz0pTBpM6A69i8hqObcg130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP548291.RA4x3chV27iPgCh0V4uUhLW3_hz0pTBpM6A69i8hqObcg130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP548291.RA4x3chV27iPgCh0V4uUhLW3_hz0pTBpM6A69i8hqObcg130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP548291.RA4x3chV27iPgCh0V4uUhLW3_hz0pTBpM6A69i8hqObcg130_provenance.
- NP548291.RA4x3chV27iPgCh0V4uUhLW3_hz0pTBpM6A69i8hqObcg130_assertion description "[Defective TGF-beta signaling in endothelial cells attributable to mutations in endoglin or the type I receptor ALK-1 leads to hereditary hemorrhagic telangiectasia, whereas defective BMP signaling attributable to mutations in the BMP receptor II has been associated with development of primary pulmonary hypertension.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP548291.RA4x3chV27iPgCh0V4uUhLW3_hz0pTBpM6A69i8hqObcg130_provenance.
- NP548291.RA4x3chV27iPgCh0V4uUhLW3_hz0pTBpM6A69i8hqObcg130_assertion evidence source_evidence_literature NP548291.RA4x3chV27iPgCh0V4uUhLW3_hz0pTBpM6A69i8hqObcg130_provenance.
- NP548291.RA4x3chV27iPgCh0V4uUhLW3_hz0pTBpM6A69i8hqObcg130_assertion SIO_000772 16675726 NP548291.RA4x3chV27iPgCh0V4uUhLW3_hz0pTBpM6A69i8hqObcg130_provenance.
- NP548291.RA4x3chV27iPgCh0V4uUhLW3_hz0pTBpM6A69i8hqObcg130_assertion wasDerivedFrom befree-2016 NP548291.RA4x3chV27iPgCh0V4uUhLW3_hz0pTBpM6A69i8hqObcg130_provenance.
- NP548291.RA4x3chV27iPgCh0V4uUhLW3_hz0pTBpM6A69i8hqObcg130_assertion wasGeneratedBy ECO_0000203 NP548291.RA4x3chV27iPgCh0V4uUhLW3_hz0pTBpM6A69i8hqObcg130_provenance.
- befree-2016 importedOn "2016-02-19" NP548291.RA4x3chV27iPgCh0V4uUhLW3_hz0pTBpM6A69i8hqObcg130_provenance.