Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP375563.RAn1XGzrLfVivSbjd01mEd_BwrCnQ6PJdilQ27O1HQjNA130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP375563.RAn1XGzrLfVivSbjd01mEd_BwrCnQ6PJdilQ27O1HQjNA130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP375563.RAn1XGzrLfVivSbjd01mEd_BwrCnQ6PJdilQ27O1HQjNA130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP375563.RAn1XGzrLfVivSbjd01mEd_BwrCnQ6PJdilQ27O1HQjNA130_provenance.
- NP375563.RAn1XGzrLfVivSbjd01mEd_BwrCnQ6PJdilQ27O1HQjNA130_assertion description "[Indeed, defects in FRAS1 and FREM2 have been identified in Fraser syndrome patients.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP375563.RAn1XGzrLfVivSbjd01mEd_BwrCnQ6PJdilQ27O1HQjNA130_provenance.
- NP375563.RAn1XGzrLfVivSbjd01mEd_BwrCnQ6PJdilQ27O1HQjNA130_assertion evidence source_evidence_literature NP375563.RAn1XGzrLfVivSbjd01mEd_BwrCnQ6PJdilQ27O1HQjNA130_provenance.
- NP375563.RAn1XGzrLfVivSbjd01mEd_BwrCnQ6PJdilQ27O1HQjNA130_assertion SIO_000772 21182980 NP375563.RAn1XGzrLfVivSbjd01mEd_BwrCnQ6PJdilQ27O1HQjNA130_provenance.
- NP375563.RAn1XGzrLfVivSbjd01mEd_BwrCnQ6PJdilQ27O1HQjNA130_assertion wasDerivedFrom befree-20140225 NP375563.RAn1XGzrLfVivSbjd01mEd_BwrCnQ6PJdilQ27O1HQjNA130_provenance.
- NP375563.RAn1XGzrLfVivSbjd01mEd_BwrCnQ6PJdilQ27O1HQjNA130_assertion wasGeneratedBy ECO_0000203 NP375563.RAn1XGzrLfVivSbjd01mEd_BwrCnQ6PJdilQ27O1HQjNA130_provenance.
- befree-20140225 importedOn "2014-02-25" NP375563.RAn1XGzrLfVivSbjd01mEd_BwrCnQ6PJdilQ27O1HQjNA130_provenance.