Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP1798.RAPaS0mWE4oY8CkhnEZPYoD_hDdORn2TkRV0brsF-Rn1c130_provenance>. }
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- source_evidence_curated type ECO_0000205 NP1798.RAPaS0mWE4oY8CkhnEZPYoD_hDdORn2TkRV0brsF-Rn1c130_provenance.
- source_evidence_curated label "DisGeNET evidence - CURATED" NP1798.RAPaS0mWE4oY8CkhnEZPYoD_hDdORn2TkRV0brsF-Rn1c130_provenance.
- source_evidence_curated comment "Gene-disease associations manually curated." NP1798.RAPaS0mWE4oY8CkhnEZPYoD_hDdORn2TkRV0brsF-Rn1c130_provenance.
- NP1798.RAPaS0mWE4oY8CkhnEZPYoD_hDdORn2TkRV0brsF-Rn1c130_assertion description "[Two common endoglin mutations in families with hereditary hemorrhagic telangiectasia in the Netherlands Antilles: evidence for a founder effect.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1798.RAPaS0mWE4oY8CkhnEZPYoD_hDdORn2TkRV0brsF-Rn1c130_provenance.
- NP1798.RAPaS0mWE4oY8CkhnEZPYoD_hDdORn2TkRV0brsF-Rn1c130_assertion evidence source_evidence_curated NP1798.RAPaS0mWE4oY8CkhnEZPYoD_hDdORn2TkRV0brsF-Rn1c130_provenance.
- NP1798.RAPaS0mWE4oY8CkhnEZPYoD_hDdORn2TkRV0brsF-Rn1c130_assertion SIO_000772 10982033 NP1798.RAPaS0mWE4oY8CkhnEZPYoD_hDdORn2TkRV0brsF-Rn1c130_provenance.
- NP1798.RAPaS0mWE4oY8CkhnEZPYoD_hDdORn2TkRV0brsF-Rn1c130_assertion wasDerivedFrom uniprot-20150221 NP1798.RAPaS0mWE4oY8CkhnEZPYoD_hDdORn2TkRV0brsF-Rn1c130_provenance.
- NP1798.RAPaS0mWE4oY8CkhnEZPYoD_hDdORn2TkRV0brsF-Rn1c130_assertion wasGeneratedBy ECO_0000218 NP1798.RAPaS0mWE4oY8CkhnEZPYoD_hDdORn2TkRV0brsF-Rn1c130_provenance.
- uniprot-20150221 importedOn "2015-02-21" NP1798.RAPaS0mWE4oY8CkhnEZPYoD_hDdORn2TkRV0brsF-Rn1c130_provenance.