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- source_evidence_literature type ECO_0000212 NP426599.RASaYzKXcVEw59jAo7ASqs_POlCRoefY0ChoX68pd8BBc130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP426599.RASaYzKXcVEw59jAo7ASqs_POlCRoefY0ChoX68pd8BBc130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP426599.RASaYzKXcVEw59jAo7ASqs_POlCRoefY0ChoX68pd8BBc130_provenance.
- NP426599.RASaYzKXcVEw59jAo7ASqs_POlCRoefY0ChoX68pd8BBc130_assertion description "[The entire coding region of connexin 26 was sequenced in 75 hearing impaired children and adults in Israel in order to determine the percentage of hearing loss attributed to connexin 26 and the types of mutations in this population.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP426599.RASaYzKXcVEw59jAo7ASqs_POlCRoefY0ChoX68pd8BBc130_provenance.
- NP426599.RASaYzKXcVEw59jAo7ASqs_POlCRoefY0ChoX68pd8BBc130_assertion evidence source_evidence_literature NP426599.RASaYzKXcVEw59jAo7ASqs_POlCRoefY0ChoX68pd8BBc130_provenance.
- NP426599.RASaYzKXcVEw59jAo7ASqs_POlCRoefY0ChoX68pd8BBc130_assertion SIO_000772 10982182 NP426599.RASaYzKXcVEw59jAo7ASqs_POlCRoefY0ChoX68pd8BBc130_provenance.
- NP426599.RASaYzKXcVEw59jAo7ASqs_POlCRoefY0ChoX68pd8BBc130_assertion wasDerivedFrom befree-20150227 NP426599.RASaYzKXcVEw59jAo7ASqs_POlCRoefY0ChoX68pd8BBc130_provenance.
- NP426599.RASaYzKXcVEw59jAo7ASqs_POlCRoefY0ChoX68pd8BBc130_assertion wasGeneratedBy ECO_0000203 NP426599.RASaYzKXcVEw59jAo7ASqs_POlCRoefY0ChoX68pd8BBc130_provenance.
- befree-20150227 importedOn "2015-02-27" NP426599.RASaYzKXcVEw59jAo7ASqs_POlCRoefY0ChoX68pd8BBc130_provenance.