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- source_evidence_literature type ECO_0000212 NP702334.RAHPlsR2oztny_e9AxBr0vrdlCknXfus6VO481ZZgLjxg130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP702334.RAHPlsR2oztny_e9AxBr0vrdlCknXfus6VO481ZZgLjxg130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP702334.RAHPlsR2oztny_e9AxBr0vrdlCknXfus6VO481ZZgLjxg130_provenance.
- NP702334.RAHPlsR2oztny_e9AxBr0vrdlCknXfus6VO481ZZgLjxg130_assertion description "[Thus, our study supports that screening for large rearrangements should be considered to improve the genetic analysis in HHT patients with no apparent mutations in ALK1 and ENG using direct sequencing.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP702334.RAHPlsR2oztny_e9AxBr0vrdlCknXfus6VO481ZZgLjxg130_provenance.
- NP702334.RAHPlsR2oztny_e9AxBr0vrdlCknXfus6VO481ZZgLjxg130_assertion evidence source_evidence_literature NP702334.RAHPlsR2oztny_e9AxBr0vrdlCknXfus6VO481ZZgLjxg130_provenance.
- NP702334.RAHPlsR2oztny_e9AxBr0vrdlCknXfus6VO481ZZgLjxg130_assertion SIO_000772 18312453 NP702334.RAHPlsR2oztny_e9AxBr0vrdlCknXfus6VO481ZZgLjxg130_provenance.
- NP702334.RAHPlsR2oztny_e9AxBr0vrdlCknXfus6VO481ZZgLjxg130_assertion wasDerivedFrom befree-20150227 NP702334.RAHPlsR2oztny_e9AxBr0vrdlCknXfus6VO481ZZgLjxg130_provenance.
- NP702334.RAHPlsR2oztny_e9AxBr0vrdlCknXfus6VO481ZZgLjxg130_assertion wasGeneratedBy ECO_0000203 NP702334.RAHPlsR2oztny_e9AxBr0vrdlCknXfus6VO481ZZgLjxg130_provenance.
- befree-20150227 importedOn "2015-02-27" NP702334.RAHPlsR2oztny_e9AxBr0vrdlCknXfus6VO481ZZgLjxg130_provenance.