Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP732555.RAPcmQb4EJzsY3KK8qnLzG_sf69Lm_ZpNIZ0feY0H1TRs130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP732555.RAPcmQb4EJzsY3KK8qnLzG_sf69Lm_ZpNIZ0feY0H1TRs130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP732555.RAPcmQb4EJzsY3KK8qnLzG_sf69Lm_ZpNIZ0feY0H1TRs130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP732555.RAPcmQb4EJzsY3KK8qnLzG_sf69Lm_ZpNIZ0feY0H1TRs130_provenance.
- NP732555.RAPcmQb4EJzsY3KK8qnLzG_sf69Lm_ZpNIZ0feY0H1TRs130_assertion description "[Endoglin (CD105), a component of the TGF-beta 1 receptor complex, is the target gene for the dominantly inherited vascular disorder hereditary hemorrhagic telangiectasia type 1 (HHT1).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP732555.RAPcmQb4EJzsY3KK8qnLzG_sf69Lm_ZpNIZ0feY0H1TRs130_provenance.
- NP732555.RAPcmQb4EJzsY3KK8qnLzG_sf69Lm_ZpNIZ0feY0H1TRs130_assertion evidence source_evidence_literature NP732555.RAPcmQb4EJzsY3KK8qnLzG_sf69Lm_ZpNIZ0feY0H1TRs130_provenance.
- NP732555.RAPcmQb4EJzsY3KK8qnLzG_sf69Lm_ZpNIZ0feY0H1TRs130_assertion SIO_000772 9366572 NP732555.RAPcmQb4EJzsY3KK8qnLzG_sf69Lm_ZpNIZ0feY0H1TRs130_provenance.
- NP732555.RAPcmQb4EJzsY3KK8qnLzG_sf69Lm_ZpNIZ0feY0H1TRs130_assertion wasDerivedFrom befree-20150227 NP732555.RAPcmQb4EJzsY3KK8qnLzG_sf69Lm_ZpNIZ0feY0H1TRs130_provenance.
- NP732555.RAPcmQb4EJzsY3KK8qnLzG_sf69Lm_ZpNIZ0feY0H1TRs130_assertion wasGeneratedBy ECO_0000203 NP732555.RAPcmQb4EJzsY3KK8qnLzG_sf69Lm_ZpNIZ0feY0H1TRs130_provenance.
- befree-20150227 importedOn "2015-02-27" NP732555.RAPcmQb4EJzsY3KK8qnLzG_sf69Lm_ZpNIZ0feY0H1TRs130_provenance.