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- NP1798.RAPaS0mWE4oY8CkhnEZPYoD_hDdORn2TkRV0brsF-Rn1c130_assertion type Assertion NP1798.RAPaS0mWE4oY8CkhnEZPYoD_hDdORn2TkRV0brsF-Rn1c130_head.
- 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.